SciCan Bravo Operator's Manual

BRAVO

AUTOCLAVES

Bravo Operator’s Manual SD-306-4-EN, Copyright 2010 SciCan Ltd. All rights reserved.

• Operator’s Manual

I..

TABLE OF CONTENTS

1. INTRODUCTION ............................................................................................................................. 1

SYMBOLS USED IN THE MANUAL ................................................................................................................... 1

DISCLAIMERS ................................................................................................................................................... 1

GENERAL WARNINGS ...................................................................................................................................... 2

2. RECEIVING YOUR BRA V O ............................................................................................................ 3

SHIPPING WEIGHT ........................................................................................................................................... 3

DESCRIPTION OF PACKAGE CONTENTS ...................................................................................................... 3

HANDLING THE UNIT ........................................................................................................................................ 4

3. PRODUCT OVERVIEW ................................................................................................................... 5

GENERAL CHARACTERISTICS ......................................................................................................................... 5

FRONT ............................................................................................................................................................... 6

REAR .................................................................................................................................................................. 7

CONTROL PANEL ............................................................................................................................................ 8

COMMAND KEYS ...................................................................................................................................... 8

LCD DISPLAY ............................................................................................................................................ 8

SAMPLE OPERATING CYCLE .......................................................................................................................... 9

4. INSTALLATION ............................................................................................................................. 10

DIMENSIONS AND WEIGHT ........................................................................................................................... 10

COMPARTMENT DIMENSIONS FOR BUILT-IN INSTALLATIONS ................................................................ 10

GENERAL INSTALLATION PRECAUTIONS .................................................................................................. 11

ELECTRICAL CONNECTIONS ........................................................................................................................ 11

CONNECTING THE DATA RECORDER ......................................................................................................... 11

CONNECTING AN EXTERNAL WATER TANK .............................................................................................. 12

DIRECT CONNECTION TO A CENTRALIZED DRAINING POINT .................................................................. 13

5. INSTRUCTIONS FOR USE ........................................................................................................... 14

TURNING ON THE UNIT ................................................................................................................................. 14

INITIAL AUTOMATIC TEST ............................................................................................................................ 14

AMBIENT PRESSURE VALUES ...................................................................................................................... 14

STAND-BY MODE ............................................................................................................................................ 15

FILLING DISTILLED WATER ........................................................................................................................... 16

Manual filling ............................................................................................................................................ 16

Automatic filling ........................................................................................................................................ 16

MAX LEVEL IN THE INTERNAL DRAIN TANK ................................................................................................ 17

6. CONFIGURATION ......................................................................................................................... 18

STARTING AND ENTERING THE SETUP MODE ........................................................................................... 18

HOW THE KEYS FUNCTION IN SETUP MODE .............................................................................................. 18

DESCRIPTION OF THE MENU ITEMS ............................................................................................................ 20

DEFAULTS SETTINGS .................................................................................................................................... 22

CONFIGURATION OPTIONS........................................................................................................................... 22

Setting the language ................................................................................................................................ 22

Setting the date ........................................................................................................................................ 22

Setting the time ........................................................................................................................................ 23

Setting the password ................................................................................................................................ 23

Setting the sterilization programs ............................................................................................................. 24

Setting the STAND-BY mode ................................................................................................................... 28

Setting the printing mode ......................................................................................................................... 29

Setting the tank filling mode ..................................................................................................................... 31

Setting the water draining mode .............................................................................................................. 31

Acquisition of the ambient pressure ......................................................................................................... 32

Adjusting the contrast of the liquid crystal display ................................................................................... 33

EXIT THE CONFIGURATION MODE .............................................................................................................. 33

TABLE OF CONTENTS

II..

7. PREPARING MATERIAL FOR STERILIZATION .......................................................................... 34

TREATING TEXTILE MATERIAL BEFORE STERILIZATION ......................................................................... 34

ARRANGING THE LOAD ................................................................................................................................. 34

8. PROGRAM SELECTION .............................................................................................................. 36

INTRODUCTION .............................................................................................................................................. 36

PROCEDURE .................................................................................................................................................. 36

9. RUNNING THE CYCLE ................................................................................................................ 38

STARTING THE CYCLE ................................................................................................................................. 38

PROGRAM EXECUTION ................................................................................................................................. 39

RESULT OF THE CYCLE ............................................................................................................................... 43

CHECKING THE CYCLE DATA REPORT (FOR UNITS WITH PRINTERS) ................................................... 44

MANUAL CYCLE INTERRUPTION .................................................................................................................. 44

RESETTING THE SYSTEM ............................................................................................................................. 45

10. STORING STERILIZE D M A T E R I AL S ......................................................................................... 46

INTRODUCTION .............................................................................................................................................. 46

HANDLING ....................................................................................................................................................... 46

STORAGE ........................................................................................................................................................ 46

11. TEST PROGRAMS ..................................................................................................................... 47

INTRODUCTION .............................................................................................................................................. 47

BOWIE & DICK TEST ...................................................................................................................................... 47

VACUUM TEST................................................................................................................................................ 48

AP P E N D I X A – TECHNICAL CHARACTERISTICS ......................................................................... 50

SUMMARY TABLE ........................................................................................................................................... 50

SAFETY DEVICES ........................................................................................................................................... 51

WATER SUPPLY CHARACTERISTICS .......................................................................................................... 52

APPENDIX B – P R O G R A M S ............................................................................................................ 53

INTRODUCTION .............................................................................................................................................. 53

PROGRAM SUMMARY TABLE ....................................................................................................................... 54

STERILIZATION PROGRAM DIAGRAM ......................................................................................................... 56

DIAGRAMS OF THE TEST CYCLES ............................................................................................................... 61

EXAMPLES OF PRINTED REPORTS ............................................................................................................. 62

APPENDIX C - MAINTENANCE ....................................................................................................... 64

ROUTINE MAINTENANCE .............................................................................................................................. 64

MAINTENANCE DESCRIPTION ...................................................................................................................... 65

Clean door gasket and porthole (door plate) ............................................................................................ 65

Clean external surfaces ........................................................................................................................... 65

Clean sterilization chamber and accessories ........................................................................................... 65

Disinfect external surfaces ....................................................................................................................... 65

Clean internal distilled water tank ............................................................................................................ 66

Clean external distilled water tank ........................................................................................................... 66

Safety valve maintenance ........................................................................................................................ 66

Clean/replace the drain filter .................................................................................................................... 66

Replace bacteriological filter .................................................................................................................... 67

Replace the door gasket .......................................................................................................................... 67

Replacing the printer paper on units equipped with internal printers ....................................................... 68

Periodic sterilizer calibration and 3000 cycle maintenance ...................................................................... 68

TABLE OF CONTENTS

III..

APPENDIX D – TROUBLESHOOTING ............................................................................................. 69

APPENDIX E – A L A R M S .................................................................................................................. 72

ALARMS ........................................................................................................................................................... 72

ALARM INTERVENTION .................................................................................................................................. 72

Alarm during a cycle ................................................................................................................................. 72

Alarm outside the cycle ........................................................................................................................... 73

RESETTING THE SYSTEM ............................................................................................................................ 74

ALARM CODES ................................................................................................................................................ 75

ANALYSIS AND RESOLUTION OF PROBL E MS ............................................................................................. 77

APPENDIX F – D I A G R A M S .............................................................................................................. 83

ELECTRICAL DIAGRAM .................................................................................................................................. 83

PLUMBING DIAGRAM ..................................................................................................................................... 84

PLUMBING DIAGRAM ..................................................................................................................................... 84

APPENDIX G - NOTES ..................................................................................................................... 85

APPENDIX H – SPARE PARTS & ACCESSORIES .......................................................................... 86

APPENDIX I – TECHNICAL SUPPORT ............................................................................................ 87

APPENDIX J – LIMITED WARRANTY .............................................................................................. 88

1. INTRODUCTION

1..

1. INTRODUCTION

SYMBOLS USED IN
THE MANUAL

Congratulations on your selection of the BravoTM Autoclave. We are confident that you have
purchased the finest equipment of its type. The Bravo is a counter-top unit that features a
number of sterilizing cycles designed to meet your needs and suitability for steam sterilization.

The details of installing, operating and maintaining your Bravo are all contained within this
operator’s manual. To ensure years of safe, trouble-free service please read these instructions
before operating this unit and keep them for future reference. Operational, maintenance and
replacement instructions should be followed for the product to perform as designed. Contents
of this manual are subject to change without notice to reflect changes and improvements to
the Bravo product.

NOTE

THIS SYMBOL INDICATES IMPORTANT INFORMATION.

WARNING

THIS SYMBOL INDICATES A POTENTIAL DANGER OF INJURY. FOLLOW
THE PROCEDURES DESCRIBED IN THE MANUAL TO AVOID INJURING
THE USER AND/OR OTHERS.

DANGER

THIS SYMBOL INDICATES A POTENTIAL DANGER OF PROPERTY
DAMAGE. FOLLOWS THE INSTRUCTIONS IN THE MANUAL TO PREVENT
POTENTIAL DAMAGE TO MATERIALS, EQUIPMENT OR OTHER
PROPERTY.

DANGER

THIS SYMBOL INDICATES A POTENTIAL DANGER DUE TO HIGH
TEMPERATURE.

DISCLAIMERS

The Bravo units described in this manual are to be used exclusively for the sterilization of solid
and hollow re-usable instruments and porous materials (e.g., textiles).

WARNING

THE DEVICE MUST ONLY BE USED BY QUALIFIED PERSONNEL. IT MAY
NOT BE USED OR HANDLED BY INEXPERIENCED AND/OR
UNAUTHORIZED PERSONNEL FOR ANY REASON.
THIS DEVICE MUST NOT BE USED FOR THE STERILIZATION OF FLUIDS,
LIQUIDS OR PHARMACEUTICAL PRODUCTS.

Do not permit any person other than certified personnel to supply parts for, service or maintain
your Bravo. SciCan shall not be liable for incidental, special or consequential damages caused
by any maintenance or services performed on the Bravo by a third party, or for the use of
equipment or parts manufactured by a third party, including lost profits, any commercial loss,
economic loss, or loss arising from personal injury.

Never remove the cover of the unit and never insert objects through holes or openings in the
cabinetry. Doing so may damage the unit and / or pose a hazard to the operator.

All elements of this book are common to Bravo17, Bravo

17V

and Bravo

21V

, except where noted.

1. INTRODUCTION

2.

GENERAL
WARNINGS

Please observe the following precautions in order to avoid injury or property damage:
– Use ONLY high quality distilled water.

WARNING

THE USE OF WATER OF INADEQUATE QUALITY CAN SEVERELY
DAMAGE THE UNIT. FOR MORE INFORMATION, SEE APPENDIX A,
TECHNICAL CHARACTERISTICS.

– Do not pour water or other liquids on the device;
– Do not pour flammable substances on the device;
– Do not use the device in the presence of gas or explosive or flammable vapors;

– Before performing any maintenance or cleaning, ALWAYS DISCONNECT the power

supply.

WARNING

WHEN IT IS NOT POSSIBLE TO DISCONNECT THE UNIT’S POWER
SUPPLY, WHEN THE EXTERNAL POWER GRID SWITCH (MAIN BREAKER)
IS FAR AWAY OR, WHEN IT IS NOT VISIBLE FROM THE UNIT, PLACE A
WORK IN PROGRESS SIGN ON THE EXTERNAL POWER GRID SWITCH
(MAIN BREAKER) AFTER TURNING IT OFF.

– Make sure the electrical system is grounded conforming to current laws and/or standards;
– Do not remove any label or nameplate from the device; request new ones, if necessary.
– Use only original replacement parts.

WARNING

FAILURE TO OBSERVE THE WARNINGS LISTED ABOVE RELEASES THE
MANUFACTURER FROM ALL LIABILITY.

2. RECEIVING YOUR BRAVO

3.

2. RECEIVING
YOUR BRAVO

SHIPPING WEIGHT

Total shipping weights :

Bravo17: approximately 126 lbs / 57 kg
Bravo

17V

: approximately 136 lbs / 62 kg

Bravo

21V

: approximately 150 lbs / 68 kg

NOTE

CHECK THE INTEGRITY OF THE PACKAGE UPON

RECEIPT.

Confirm that:
– the contents match the specifications of the order (see the

accompanying document);

– there is no obvious damage to the contents.

NOTE

IF YOU HAVE RECEIVED THE WRONG PRODUCT, ARE MISSING P A RTS, OR IF YOUR UNIT

HAS ANY TYPE OF DAMAGE, IMMEDIATELY PROVIDE A DETAILED DESCRIPTION TO THE
SELLER AND SHIPPER.

DESCRIPTION OF
PACKAGE
CONTENTS

The package contains:
– Bravo Steam sterilizer

1. Stainless steel wire instrument tray (3 pc with Bravo17, 5pc with Bravo

17V

, Bravo

21V

);

2. Stainless steel rack;

3. Instruction/Operators manual and other documents;

4. Tray extractor;

5. Container with quick connect for adding distilled water (about 0.5 US gal / 2 L );

6. Extra bacteriological filter;

7. Silicone tube (6.5 ft / 2 m) for draining water, with quick connector;

8. Bravo

17V

and Bravo

21V

models include spare roll of printer paper;

9. Chamber drain filter

10. Chamber drain filter wrench

NOTE

THE CUSTOMER MUST KEEP THE PURCHASE RECEIPT FOR ANY WAR RANTY SERVICE.

2. RECEIVING YOUR BRAVO

4.

HANDLING THE
UNIT

Where possible, the packaged product must be handled using suitable mechanical means and
following the instructions shown on the package.
In the case of manual handling, the product must be lifted by two people using the handles cut
in the side of the box.

Once removed from the box, the unit must be lifted by two people and transported on a cart or
other similar device.

WARNING

WE RECOMMEND THAT THE UNIT BE TRANSPORTED AND STORED AT A
TEMPERATURE NO LOWER THAN 5 °C. PROLONGED EXPOSURE TO
LOW TEMPERATURES COULD DAMAGE THE PRODUCT.

NOTE

KEEP THE ORIGINAL PACKAGING AND USE IT WHEN THE DEVICE IS TRANSPORTED. USING

DIFFERENT PACKAGING COULD DAMAGE THE PRODUCT DURING SHIPPING.

DANGER

BEFORE SHIPPING, DRAIN THE DISTILLED WATER AND USED WATER
TANKS, AND ENSURE THE DEVICE HAS BEEN OFF FOR 30 MINUTES
FOLLOWING ITS LAST CYCLE SO THAT THE ALL THE HOT INTERNAL
PARTS WILL HAVE TIME TO COOL.

3. PRODUCT OVERVIEW

5.

3. PRODUCT
OVERVIEW

Bravo is SciCan's revolutionary chamber autoclave designed with safety, performance,
flexibility and ease of use in mind.

It is a sophisticated yet easy-to-use sterilizer with a wide range of configuration options and
patented operating devices designed to satisfy every need for sterilizing medical and dental
tools, guaranteeing the maximum performance under all conditions.

Easy-to-use, compact and aesthetically pleasing, Bravo is the ideal partner for professionals
seeking maximum sterilization safety

GENERAL
CH A R A C T E R I S T I CS

Bravo is a microprocessor-controlled steam sterilizer with a large sterilization chamber made
of stamped stainless steel.

It is characterized by an advanced fractionated vacuum system for the complete removal of air
from hollow and porous materials, and an effective final vacuum drying phase capable of
effective drying of these loads.

Its exclusive steam generation system, effective plumbing circuit and electronic management
(supplemented by high-precision sensors) guarantees high process execution speeds and
excellent thermodynamic parameter stability. Moreover, its Process Evaluation System
constantly monitors all the machine's vital parameters in real-time, guaranteeing absolute
safety and perfect results.

It offers users 10 sterilization programs (one customizable), each equipped with optimized
drying for the fast, effective sterilization of the various types of loads (instruments and
materials) used in a medical or dental environment. The custom programs have not been
validated and have not been cleared in the U.S. by FDA for healthcare use.

Bravo units also offer a number of interesting options for configuring the preheating mode
(based on the sterilizer's frequency of use) and printing the cycle report (printer optional on
Bravo17).

Bravo sterilizers also have one of the most complete, sophisticated and advanced safety
systems available today to protect users in the case of electrical, mechanical, or thermal
operating anomaly.

NOTE

PLEASE REFER TO APPENDIX A (TECHNICAL CHARACTERISTICS) FOR A DESCRIPTION

OF BRAVO’S INTEGRATED SAFETY DEVICES.

3. PRODUCT OVERVIEW

6.

FRONT

LCD display and
control panel

Service compartment
access panel

Door

Printer paper
output slot (printer
optional on
Bravo17)

On/Off switch

Bacteriological filter

Sterilization
chamber

Door microswitch

Distilled water fill quick connect
Door

Used water drain quick
connect

Water drain filter

Service compartment
(shown open)

Built-in printer
(optional in Bravo17)

Motorized
closing system

RS232 serial port

(Manufacture use only)

3. PRODUCT OVERVIEW

7.

REAR

Distilled water tank vent
hole

Safety valve

Heat exchanger

Mains fuses

Power cord

Band heating element safety thermostat and manual
rearm

Connection for directly draining the
used water tank

Connection for automatically filling the
distilled water tank

Steam generator safety thermostat and manual rearm

Jack socket for the
external tank level
sensor

Distilled water tank
draining point

Signal input for future
Bravo Pure Start/Stop

Ventilation Outlets
(back and side of unit)

3. PRODUCT OVERVIEW

8.

CONTROL
PANEL

COMMAND KEYS

LCD DISPLAY

Command keys will perform different functions depending on the mode:

Key

NORMAL mode

SETUP mode

Cycle Start/Stop

Enter, confirmation of the value/option
selected

Sterilization cycle selection

Value increment / Forward scroll of
the menu options

Test cycle selection

Value decrement / Backward scroll of
the menu options

Enter Setup mode

ESC, quit the current menu

LCD Display
Command keys

4 lines of 20 characters

Illuminated icons

Door status

Water level

Process status

Setup status

Alarm

3. PRODUCT OVERVIEW

9.

SAMPLE
OPERATING
CYCLE

The Bravo’s sterilization program is a succession of phases, each with a specific purpose.
After loading the material in the chamber, closing the door, selecting the program and starting

the cycle (the door opening mechanism locks automatically), the standard program (for porous
materials, 134 °C at 4 minutes, for example) uses the following sequence:

1. Preheats the generator and sterilization chamber;

2. Removes the air and penetrates the material by steam through a series of vacuum
(extracting fluid from the sterilization chamber) and pressure (injecting steam into the
chamber) phases;

3. Raises the pressure, with the consequent increase in the temperature of the steam, until
reaching the conditions required for sterilization (for example, 134 °C);

4. Stabilizes the pressure and temperature;

5. Sterilizes for the required time (for example, 4 minutes);

6. Depressurizes the sterilization chamber;

7. Begins vacuum-drying phase;

8. Ventilates the load with sterile air;

9. Brings the pressure of the sterilization chamber back to the atmospheric level.

After reaching atmospheric pressure, the door is automatically unlocked and can be opened to
remove the load from the sterilization chamber.

Phases 1, 3, 4, 6 and 9 are identical in all cycles, with slight variations of duration that are
solely dependent on the quantity and consistency of the load and the heating conditions of the
sterilizer. Phases 2, 5, 7 and 8, however, vary their configuration and/or duration on the basis
of the cycle selected (and, consequently, the type of load) and the choices made by the user.

NOTE

PLEASE REFER TO APPENDIX B (PROGRAMS) FOR MORE DETAIL.

4. INSTALLATION

10.

4. INSTALLATION

DIMENSIONS AND
WEIGHT

Correct and careful installation will ensure your Bravo functions properly, protects operators
from physical injury and protects property from damage.

– Height (all models) 16.5” / 420 mm
– Width (all models) 19” / 480 mm
– Depths (excluding rear connections)

Bravo17, Bravo

17V

22.0” / 560 mm

Bravo

21V

25.0” / 635 mm

– Total weights (with rack and trays)

Bravo17: 121 lbs / 55 kg
Bravo

17V

: 128 lbs / 58 kg

Bravo

21V

: 139 lbs / 63 kg

Electricity

The electrical system to which the sterilizer will be connected must accommodate the electrical
characteristics of this device. This information is shown on the back of the machine.

COMPARTMENT
DIMENSIONS FOR
BUILT-IN
INSTALLATIONS

When installing the sterilizer inside a cabinet, you
must provide adequate space all around the device
to provide effective ventilation. There should also be
an opening in the back large enough to provide
adequate air flow. This will allow optimum cooling of
the heat exchanger.

A built-in compartment MUST have the minimum
dimensions shown in the figure at right.

– Height (all models) 18.5” / 490 mm
– Width (all models) 23” / 580 mm
– Depths

Bravo17, Bravo

17V

26” / 660 mm

Bravo

21V

29” / 735 mm

WARNING

COMPARTMENT DIMENSIONS LESS THAN THOSE SHOWN M AY
COMPROMISE THE CORRECT CIRCULATION OF AIR AROUND THE
DEVICE AND MAY NOT PROVIDE ADEQUATE COOLING. THIS CAN
RESULT IN THE DETERIORATION OF PERFORMANCE AND/OR POSSIBLE
DAMAGE.

NOTE

DO NOT REMOVE THE UPPER COVER OR ANY OTHER EXTERNAL PART. WHEN INSTALLED

IN THE COMPARTMENT, THE DEVICE MUST BE COMPLETE WITH ALL ITS P A RTS.

PLEASE REFER TO APPENDIX A (TECHNICAL CHARACTERISTICS) FOR COMPLETE

TECHNICAL DATA.

4. INSTALLATION

11.

GENERAL
INSTALLATION
PRECAUTIONS

To ensure operator safety and the correct performance of the device:

– Install the sterilizer on a flat level surface strong enough to support the device's weight,

and use the leveling feet to compensate for an irregular surface.

– Leave adequate space for ventilation, at least 2” (50 mm) on both side and top and 4”

(100mm) at the back. If the device is installed in a cabinet, be sure to respect the warnings
in the preceding paragraph, avoiding any obstructions to the air intake.

– Avoid contact with water or liquids. Do not install the sterilizer near tubs, sinks or similar

places, as this could cause short circuits and/or potentially dangerous situations for the
operator.

– Do not install the sterilizer in a place that is excessively humid or poorly ventilated;
– Do not install the machine were there is gas or flammable and/or explosive vapors;
– Install the device so that the power cord is not sharply bent or kinked. It must run freely to

the electrical connection socket.

– Install the device so that any external fill/drain tubing(s) is/are not sharply bent or kinked.

These must run freely to the drain tank.

ELECTRICAL
CONNECTIONS

The Bravo must be connected to an outlet that provides adequate capacity for the device's
absorption and ground, and which conforms with current laws and/or standards. The outlet
must also be protected by suitable breaker.

WARNING

THE MANUFACTURER WILL NOT BE LIABLE FOR DAMAGES CAUSED BY
INSTALLING THE STERILIZER ON AN INADEQUATE ELECTRICAL
SYSTEM OR ONE NOT EQUIPPED WITH A GROUND.

If it is necessary to replace the plug on the power cord, use one with equal characteristics or,
at any rate, adequate to the device's electrical characteristics. The user is entirely responsible
for the selection and replacement of the plug. This replacement should only be performed by
a trained service professional.

NOTE

ALWAYS CONNECT THE POWER CORD DIRECTLY TO THE SOCKET. DO NOT USE

EXTENSION CORDS, ADAPTERS OR OTHER ACCESSORIES.

CONNECTING THE
DATA RECORDER

Installation

The sterilizer can be connected to external data recorder to allow the recording of the cycle
data on to a USB memory stick which can then be downloaded to a PC for archiving and
management.

The connectors in the service compartment are used for interfacing.

1. Switch off the sterilizer and open the service compartment door;

2. Insert both ends of the 9-pin connector into the serial ports of the data recorder and the

Bravo unit and secure them with the screws.
The serial port of the autoclave can be found next to the biological filter;

3. Insert the power connector pin in to the data recorder and then plug in the power

supply;

4. Fully insert the USB stick in to data recorder.

5. Switch on the sterilizer.

4. INSTALLATION

12.

CONNECTING AN
EXTERNAL
WATER TANK

To avoid having to regularly fill the internal water tank (see Chapter 5 - Instructions for Use), it
is possible to connect the sterilizer to an optional external tank that the user will less frequently
fill, or to a commercially-available, water purification system with accumulation tank.

With this option, the autoclave automatically activates a pump that fills the internal tank when it
reaches the MIN level. Be sure to monitor the external tank as the Bravo unit can not monitor
the water level in the external tank.

To connect the external tank, follow the instructions below:
– Install the tap provided on the tank; use Teflon tape or connector sealant for a perfect seal.

– Use the tank’s silicone tube (or other suitable tube) and insert it on the filling connector

taking care to push it completely on.
– Lock the tube to connector with the plastic tie provided.
– Insert the other end of the tube on the tap of the tank.
– Make sure that the tube runs freely from the device to the tank, without being bent, crushed

or obstructed in any way.
– Loosen the cap to facilitate the flow of water.
– Open the tap on the filling tank.

NOTE

REFER TO CHAPTER 6 - CONFIGURA TI ON – SETTING THE TANK FILLING MODE.

4. INSTALLATION

13.

DIRECT
CONNECTION TO A
CENTRALIZED
DRAINING POINT

Follow the instructions shown below for a correct direct connection to a centralized draining

point:

– Insert the silicone tube (provided) or other suitable plastic tube onto hose connection A;

push the tube all the way on and lock with the plastic tie or other means;

– Cut the tube to measure, push the free end on the connection provided on the centralized

draining point and lock with the plastic tie or other means;

NOTE

MAKE SURE THE TUBE IS NOT BENT, KINKED OR OBSTRUCTED IN ANY WAY.

The following diagram depicts the ideal arrangement of components:

A

Clip

Was her

Clip

Pipe

To the centralized
draining point

Centralized
draining point

Support plane

This point must be at level lower
than the sterilizer ’s support plane

NOTE

THE CONNECTION POINT TO THE CENTRAL DRAIN MUST BE LOWER THAN THE

STERILIZER'S SUPPORT SURFACE, OTHERWISE THE TANK MAY NOT EMPTY CORRECTLY.

5. INSTRUCTIONS FOR USE

14.

5. INSTRUCTIONS
FOR USE

TURNING ON THE
UNIT

Once the sterilizer has been correctly installed, it may be turned on and prepared for use.
Turn on the Bravo using the main (luminous) switch located on the right side of the unit.

NOTE

DO THIS WITH THE STERILIZER'S DOOR OPEN.

INITIAL
AUTOMATIC
TEST

When turned on, the control panel lights up and beeps so you can visually check its correct
operation. The panel then displays the message:

BRAVO17
R. Exxxx/BMyyyyyy

DEVICE CHECK- UP

NOTE

IF THE DOOR IS CLOSED, THE TEST IS INTERRUPTED. THE PANEL WILL BEEP AND

DISPLAY THE FOLLOWING MESSAGE.

OPEN DOOR

TO CONTINUE

Open the door to allow the test to continue. At the end of the test you will see:

BRAVO17
R. Exxxx/BMyyyyyy

CHECK- UP COMPLETE

AMBIENT
PRESSURE
VALUES

The sterilizer measures the ambient pressure for the correct operation of several auxiliary
devices. Whenever the difference between the value read and that previously stored is higher
than a set value, the system automatically updates the stored value after a brief delay.
Otherwise, the data remains unchanged without updating. (see Chapter 6 – Configuration ­Acquisition of the ambient pressure)
After updating, the device performs the initial automatic test procedure (see above). At the
end, the display shows the following message (accompanied by a beep):

AMBIENT PRESSURE

VALUE UPDATED

- 0.01 bar
↵ to continue

When ↵ is pressed, the device goes to STAND-BY mode (see below).

NOTE

FOR MORE INFORMATION, SEE CHAP TER 6 – CONFIGURATION - ACQUISITION OF THE

AMBIENT PRESSURE.

5. INSTRUCTIONS FOR USE

15.

STAND-BY MODE

After the initial test, the sterilizer goes into STAND -BY mode and the display shows:

Counter xxxxx/yyyyy
Stand- by HIGH

23.6 °C 30/08/02

- 0.01 bar 18:13:05

The upper line is the cycle counter. It shows the number of sterilizations performed, with the

correctly completed cycles on the left and the total number started on the right. The line below

shows the Stand-by status and the preheating mode (High-Low-Off). The two lower lines show

the temperature and pressure of the sterilization chamber on the left and current date and

time on the right.

NOTE

A CYCLE BEGINS WITH THE START OF THE STERILIZATION CYCLE (FIRST VACUUM

PHASE), EXCLUDING THE PREHEATING PHASE. A CYCLE ENDS AT THE END OF THE
PROGRAM (SEE THE CHAPTE R 9 - RUNNING THE CYCLE - PROG RAM EXECUTION).

TO SET THE DATE AND TIME AS WELL AS SELECT THE PREHEATING MODE, PRINT THE

DATA AND FILL THE TANK, PLEASE REFER TO THE CHAP T ER 6.

At regular intervals, the first two lines on the display alternate with the modes set for printing

(OFF/ON) and filling (Manual/Automatic):

Print OFF
Filling MANUAL

23.6 °C 30/08/02

- 0.01 bar 18:13:05

The icons in the lower part of the LCD screen remain off with the exception of the door status

and/or water level indicators, which light-up if the door is closed and/or the level in the filling

tank reaches its MIN or MAX values (or the MAX value in the drain tank).

During the first start-up, the MIN water level icon in the filing tank is normally on.

The device waits for the selection of the desired sterilization program (see Chapter 8 -

Program Selection).

DANGER

WHEN THE DOOR IS OPEN IN STAND-BY MODE, A BEEP INDICATES
THAT THE SURFACES INSIDE THE DEVICE ARE HOT. TO AVOID
BURNS, TAKE CARE NOT TO TOUCH THE STERILIZATION CHAMBER,
THE SUPPORTS PROVIDED OR THE INSIDE OF THE DOOR WITH YOUR
BARE HANDS.

5. INSTRUCTIONS FOR USE

16.

FILLING DISTILLED
WATER

Manual filling

Automatic filling

The first time the sterilizer is used or when the MIN water level indicator comes on, you will
have to fill, or top-off, the internal distilled water tank.

With reference to the figure (and with the door open), follow these steps:

1. Fill the manual container (2 litres/ 0.52 US gal)

with distilled water, keeping it horizontal.

2. Connect the tube’s quick connector to the

corresponding female connector under the

chamber entrance (marked ), pushing until

you hear a click.

3. Place the container in a vertical position and

loosen the cap and taking care not to spill water

on the machine.

4. The water will begin to flow into the tank.

5. Continue filling until the MIN level indicator turns off or the MAX level indicator turns on.

6. At this point, lower the bottle below the connection point on the unit, keeping it horizontal.

7. While pinching the tube with your fingers press the metal lever on the side of the connector

and detach the quick connector.

8. Refill the container (2 litres/ 0.52 US gal) and repeat steps 2, 3 and 4 a second time until

the MAX level icon appears on the display.

9. When the MAX level icon comes on (accompanied by a beep), stop filling and detach the

quick connector as described in steps 6 and 7.

NOTE

THE MAX ICON DOES NOT HAVE TO BE ON TO START A STERILIZATION PROGRAM.
THERE IS SUFFICIENT WATER IF THE MIN INDICATOR IS OFF.

DO NOT CONTINUE TO FILL ONCE M AX ICO N APP E ARS AND YOU HEAR A BEEP. DOING

SO MAY CAUSE WATER TO DRAIN FROM THE UNIT’S WATER TANK DRAINING POINT AT THE
BACK OF THE MACHINE.

If a unit is set up for automatic filling from an external tank, the filling will occur automatically
after this automatic filling option has been selected.

NOTE

USE ONLY HIGH QUALITY DISTILLED WATER. FOR WATER SPECIFICATIONS, SEE
APPENDIX A (TECHNICAL CHARACTERISTICS).

To set the automatic filling option, please refer to the Chapter 6 - Configuration – Setting the
tank filling mode.

WARNING

THE AUTOMATIC FILLING SYSTEM MUST NEVER RUN DRY. THIS WILL
CAUSE PREMATURE WEAR TO THE AUXILIARY WATER-INJECTION
PUMP. PERIODICALLY CHECK THE WATER LEVEL IN THE EXTERNAL
TANK.
IF AUXILARY WATER-INJECTION PUMP RUNS DRY, THIS MAY BE AN
INDICATION OF AN EMPTY EXTERNAL WATER TANK, AND THE UNIT
WILL DISPLAY A CYCLE FAULT A040. TURN OFF THE POWER TO THE
UNIT AND FILL THE EXTERNAL BOTTLE WITH DISTILLED WATER. THEN
TURN THE UNIT POWER ON.

5. INSTRUCTIONS FOR USE

17.

MAX LEVEL IN THE
INTERNAL DRAIN
TANK

Emptying the internal
tank

When the water level in the internal drain tank reaches the MAX level, the LCD display

alternatively flashes the MAX and MIN icons.

NOTE

AT THIS STAGE, THE UNIT WILL GENERATE AN ALARM INDICATION (SEE APPENDIX E -
ALARM S) SHOULD YOU ATTEMPT TO ST ART A STERILIZATION CYCLE.

When this occurs, empty the internal and/or external draining tank.

To drain the internal tank, follow these steps :

1. Arrange an empty container on the floor near the
sterilizer and put the free end of the supplied tube
into the container.

2. Connect the quick connector to the corresponding
female connector under the chamber entrance

(marked ), pushing until you hear a click.

3. Wait for the internal tank to drain completely, then
while pinching the tube with your fingers, press the
metal lever located on the side of the connector
and detach the quick connector.

6. CONFIGURATION

18.

6.
CONFIGURATION

Bravo users can configure the device to meet their specific needs. For example, the device's

performance may be adapted on the basis of the type of activity, the type of material to be
sterilized or its frequency of use.

The SETUP program allows selecting from several options that users can activate through an
easy-to-use menu.

NOTE

USE THE SETUP PROGRAM WHEN NECESSARY. A CORRECTLY PERSONALIZED DEVICE

PROVIDES THE BEST PERFORMANCE.

SCICAN CUSTOMER SUPPORT (SEE APPENDIX Z) IS AVAILABLE TO HELP USERS BY

PROVIDING SUGGESTIONS OR ADVICE ON THE BEST WAY TO USE THE OPTIONS IN THE

SETUP PROGRAM.

STARTING AND
ENTERING THE
SETUP MODE

To enter the SETUP mode, hold down the ⇑ key on the control panel for several seconds, until
the display reads “INSERT PASSWORD”. Enter the password “- - - - - - - -“ (8 x )
then press the ↵ key to enter the SETUP mode

INSERT PASSWORD
********

↵ to continue
⇑ to exit

Bravo17
SETUP

↵ to continue
⇑ to exit

NOTE

THE ICON SETUP ON THE DISPLAY WILL LIGHT UP AND STAY ON FOR THE ENTIRE

CONFIGURATION PHASE.

Press the ↵ key to enter the SETUP mode. The screen shows the first-level menu items (see
SETUP flowchart below).

Pressing the ESC key ⇑ quits the SETUP program and takes you back to normal operation
(stand-by mode).

NOTE

THE SETUP PROGRAM CAN ONLY BE STARTED IN S TAND-BY MODE. IT IS NOT

ACCESSIBLE DURING STERILIZATION OR TEST CYCLES.

HOW THE KEYS
FUNCTION IN
SETUP MODE

In SETUP mode the control panel keys have different functions than in normal mode.

Key

SETUP mode

ENTER key to confirm the selected option or value

Increases the value /scroll down

Decreases the value /scroll up the menu items

ESC key to exit the selected menu option

6. CONFIGURATION

19.

6. CONFIGURATION

20.

DESCRIPTION OF
THE MENU ITEMS

MAIN MENU

The main menu has six entries that allow access to additional (second-level) menus:

BASIC (basic options)
ADVANCED (advanced options)
SPECIAL (special options)

SERVICE (technician menu not accessible to users)

DATA REVIEW (summary of options selected)
EXIT SETUP (exit the SETUP program and return to normal operation.

For more info, see Exiting the SETUP program)

BASIC Menu

The Basic menu (basic options) consists of the following items:

LANGUAGE (language setting)
DATE SETTING (setting the current date)
TIME SETTING (setting the current time)
PASSWORD (setting the password)
EXIT (exit the BASIC menu and return to the main menu)

ADVANCED Menu

The Advanced menu (advanced options) consists of the following items:

PROGRAMMES (setting preselected sterilization programs, shown on the

LCD display)

STAND-BY OPTIONS (stand-by mode settings)
PRINT OPTIONS (setting printer and printing options)
FILLING OPTIONS (setting modes for filling the distilled water tank)
DRAIN OPTIONS (setting the modes for emptying the used water tank)
EXIT (exit the ADVANCED menu and return to the main menu)

SPECIAL Menu

The Special menu (special options) consists of the following items:

AMBIENT PRESSURE (acquisition of the ambient pressure)
LCD CONTRAST (adjusting the contrast of the Liquid Crystal Display)
EXIT (exit the SPECIAL menu and return to the main menu)

SERVICE Menu
The Service menu can ONLY be accessed by a SciCan technician.

DATA REVIEW Menu

The Data Review displays a summary of the device's current settings, allowing users to
verify their accuracy.

It has the following screens (shown by way of example):

6. CONFIGURATION

21.

Firmware version

Use the keys + / - to scroll through the menu.

Use the keys + / - to scroll through the menu.

Use the keys + / - to scroll through the menu.

Use the keys + / - to scroll through the menu.

Use the keys + / - to scroll through the menu.

EXIT
DATA REVIEW

↵ to continue

Press ↵ to confirm

NOTE

TO LEARN MORE ABOUT ANY O F THE TERMS AB OVE, SEE CHAP TER 6 - CONFIGURATION

- CONFIGURATION OPTIONS.

3rd PRESET
134 SOLID/WRAPPED

EXTRA DRYING +05

4th PRESET
134 EMERGENCY

FAST DRYING

1st PRESET
134 POROUS/WRAPPED

STANDARD DRYING

2nd PRESET
134 HOLLOW/UNWRAP.

FAST DRYING

Stand- by option
HIGH

120 min

Print option
OFF

1 COPY(ies)

Filling option
AUTOMATIC
Drain option
INTERNAL

BRAVO17
R. Exxxx/BMyyyyyy
LANGUAGE
ENGLISH

DATE
dd/mm/yyyy
TIME
hh:mm:ss

6. CONFIGURATION

22.

DEFAULTS
SETTINGS

The sterilizer leaves the factory with the following settings:

PROGRAMS: Preset 1: 134 POROUS/WRAPPED
Preset 2: 134 HOLLOW/UNWRAP
Preset 3: 134 SOLID/WRAPPED
Preset 4: 134 SOLID/UNWRAP

STAND-BY MODE: HIGH (preheating)
PRINT OPTIONS: OFF or 1 copy
FILLING OPTIONS: MANUAL
DRAIN OPTIONS: INTERNAL

CONFIGURATION
OPTIONS

Setting the language

(LANGUAGE on the
BASIC Menu)

To configure the unit access the SETUP mode from the stand-by screen, enter the SETUP
mode by holding down the ⇑ key on the control panel for several seconds until the SETUP
screen appears (shown below).

Counter xxxxx/yyyyy
Stand- by HIGH

23.6 °C 30/08/02

- 0.01 bar 18:13:05

Scroll to the BASIC menu and press the ↵ key. From here, scroll and select any of the
following configuration options.

Select LANGUAGE using the ↵ key. The following screen will appear:

→ ITALIANO +
ENGLISH ↑
FRANÇAIS ↓

DEUTSCH -
ESPAÑOL

Select the desired language. Move using the + or – keys and confirm using the ↵ key to store
the selection. After the data is confirmed, return to the second-level menu.

NOTE

AS SOON AS THE SELECTION IS CONFIRMED, ALL THE MENUS OF THE SETUP PROGRAM

WILL BE DISPLAYED IN THE LANGUAGE SET.

Setting the date

(DATE SETTING on the
BASIC Menu)

When DATE SETTING is selected with the ↵ key, you will see:

dd/mm/yyyy
+/- to set

↵ to enter
⇑ toexit

6. CONFIGURATION

23.

Setting the time

(TIME SETTING on the
BASIC menu)

To set the date, follow these steps:
– When the day flashes: set the current date with the + and - keys. Confirm with ↵.

– When the month flashes: set the current month with the + and - keys. Confirm with ↵.
– When the year flashes: set the current year with the + and - keys. Confirm with ↵.

The date is stored. Once the last confirmation is given, you return to the second-level menu.
When TIME SETTING is selected with the ↵ key, you will see:

hh:mm:ss
+ / - to set

↵ to enter
⇑ to exit

Follow these steps:
– When the hours flash: set the current hour with the + and - keys. Confirm with ↵.

– When the minutes flash: set the current value with the + and - keys. Confirm with ↵.

When the last confirmation is given, return to the second-level menu.

Setting the password

(PASSWORD on the
BASIC menu)

When PASSWORD is selected with the ↵ key, you will see this menu:

→ DISABLED +
ANY POWER ON ↑
ANY CYCLE START ↓

EXIT -

Select DISABLED to use the device freely, without limiting operator access.
Select ANY POWER-ON to password protect the main power switch. This allows only

authorized personnel to turn the unit on. Once it is on, it can be used by any operator.
Select ANY CYCLE START to password protect the unit both at power-on and at the start of

every sterilization program. In this mode, only authorized personnel will be able to use it.
When the ANY POWER-ON or ANY CYCLE START options are selected, the following
screen is displayed:

INSERT PASSWORD

↵ to enter
⇑ to exit

Enter the password with the + and – keys (fixed length, 8 characters).
Confirm with the ↵ key. Then, the following message will appear:

CONFIRM PASSWORD

↵ to enter
⇑ to exit

Enter the password again using the + and – keys.
Confirm with the ↵ key.

6. CONFIGURATION

24.

NOTE

TO CHANGE THE PASSWORD, FIRST SELECT THE DISABLE OPTION, WHICH CANCELS

THE PREVIOUS PASSWORD, AND THEN SELECT THE ANY POWER-ON OR ANY

CYCLE START OPTION, ENTERING THE NEW PASSWORD AS DESCRIBED ABOVE.

Setting the sterilization
programs

(PROGRAMS on the
ADVANCED menu)

Setting and storing customized sterilization programs in the four pre-set positions can be
completed by following these steps, starting in the advanced menu.
Each pre-set position can be associated to a standard or user configurable cycle (CUSTOM).

To associate a standard program and define several of its parameters, proceed as follows:

1. Select PROGRAMS using the ↵ key; the following menu appears:

→ 1st PRESET +
2nd PRESET ↑
3rd PRESET ↓

4th PRESET -
EXIT

Define the position (1, 2, 3 or 4) to which the sterilization program will be associated using
the + and - keys. Confirm with the ↵ key.

2. From here, you enter the list of available cycles:

→ 134 H OLLOW/UNWRAP.+

1 21 HOLLOW/UNWRAP.↑
134 SOLID/UNWRAP. ↓

121 SOLID/UNWRAP. -
134 EMERGENCY
134 SOLID/WRAPPED
121 SOLID/WRAPPED
134 POROUS/WRAPPED
121 POROUS/WRAPPED
XXX CUSTOM
EXIT

Using the + and - keys, scroll the list until you identify the sterilization program desired.

3. Confirm the selection with the ↵ key.

6. CONFIGURATION

25.

As a function of the choices made, you will go to one of two alternative menus that allow you to

choose the type of drying you want associated with the selected program.

a) Programs with short drying (HOLLOW/UNWRAP., SOLID/UNWRAP., EMERGENCY):

→ STANDARD DRYING +

FAST DRYING ↑
EXIT ↓

-

The default setting is STANDARD mode. Move using the + and - keys and confirm with the
↵ key.

NOTE

THE EMERGENCY PROGRAM PROVIDES ONLY FAST DRYING (SUITABLE FOR A LOAD

UP TO 0.5 KG/1.1 LBS).

b) Programs with long drying (POROUS/WRAPPED, SOLID/WRAPPED, EXTRA):

→ STANDARD DRYING +

INTELL. DRYING ↑
EXTRA DRYING ↓

EXIT -

The default setting is STANDARD. Also available are the INTELLIGENT option, an
automatic drying that adjusts its duration on the basis of the volume and/or quantity and
type of load, and the EXTRA option, a selectable value extended drying recommended for
critical loads. Move using the + and - keys and confirm with the ↵ key.

WARNING

THE FAST, INTELLIGENT A N D EXTRA DRYING OPTIONS HAVE NOT BEEN

V A L I D A T E D A N D H A V E N OT BEEN CLEARED IN THE U.S. BY FDA FOR
HEALTHCARE USE.

PLEASE REFER TO THE “PROGRAM SUMMARY T ABLE” AND ITS GENERAL
NOTES (SEE APPENDIX B – PROGRAMS) FOR A DESCRIPTION OF THE DRYING OPTIONS

AND THE MAXIMUM STERILIZABLE MASS ALLOWED IN EACH STERILIZATION PROGRAM.

When the EXTRA option is activated, the following screen appears:

EXTRA: XX min
+/- to set

↵ to enter
⇑ to exit

This option permits adding between 1 and 15 minutes of extra drying time to the
STANDARD DRYING time). Set the value using the + and - keys and confirm the selection
with the ↵ key.

NOTE

THE SELECTION CAN BE CHANGED AT ANY TIME BY FOLLOWING THE PROCEDURE

DESCRIBED ABOVE.

WHEN AN IDENTICAL STERILIZATION PROGRAM IS ALREADY PRESENT IN ANOTHER

POSITION, THE SELECTION IS NOT ACCEPTED. THE FOLLOWING WARNING APPEARS ON
THE DISPLAY, ALONG WITH A BEEP:

THIS PROGRAM
IS ALREADY PRESET

6. CONFIGURATION

26.

To define the CUSTOM program. follow these steps:

1. From the PROGRAMS menu, select the number to which the program is to be associated
(see the previous description) and then select CUSTOM in the next screen. The following
menu will appear:

→ 134°C PROCESS +

121° C PROCESS ↑
EXIT ↓

-

Select 121 °C to perform a custom program with a sterilization process at 121 °C or 134 °C
for one at 134 °C. Move using the + and - keys and confirm with the ↵ key.

2. You will then go the screen:

TIME: XX min
+/- to set

↵ to enter
⇑ to exit

Use the + and - keys to set the duration of the sterilization process and confirm with the ↵
key.

NOTE

THE DURATION OF THE STERILIZATION PROCESS IS VARIABLE FROM 4 TO 30 MINUTES

FOR THE PROGRAM AT 134 °C, AND FROM 20 TO 30 MINUTES FOR THE PROGR AM A T

121 °C.

3. After selecting the time, a new screen will ask you to specify the type of initial vacuum:

→ FRACTION. VACUUM +

SINGLE VACUUM ↑
EXIT ↓

-

Select FRACTION to perform a fractionated vacuum (for hollow bodies and porous
materials), or SINGLE for a single preliminary vacuum phase (for solid instruments). Move
using the + and - keys and confirm with the ↵ key.

4. After selecting the vacuum, a new screen will ask you to set the drying mode:

→ SHORT DRYING +

LONG DRYING ↑
EXIT ↓

-

Select LONG drying for porous and/or wrapped loads, or SHORT if you need to sterilize
solid, loose materials (and even hollow, as long as it is not wrapped). Move with the + and

- , confirm with the ↵ key.

6. CONFIGURATION

27.

5. Depending on the selection (LONG or SHORT) one of two different menus will open (these

menus are the same for the standard cycles), i.e.:
In SHORT mode the following is displayed:

→ S TANDARD DRYING +

FAST DRYING ↑
EXIT ↓

-

In LONG mode the following is displayed:

→ STANDARD DRYING +

INTELL. DRYING ↑
EXTRA DRYING ↓

EXIT -

For the choice criteria, refer to instructions on page 27.

When the CUSTOM program is already present in another position, the selection is
not accepted. The following warning appears on the display, along with a beep:

THIS PROGRAM IS
ALREADY PRESET

WARNING

CUSTOM PROGRAMS HAVE NOT BEEN VALIDATED AND HAVE NOT BEEN

CLEARED IN THE U.S. BY FDA FOR HEALTHCARE USE. THEY SHOULD ONLY
BE USED BY EXPERIENCED USERS.

PLEASE REFER TO THE “PROGRAM SUMMARY T ABLE” AND ITS GENERAL
NOTES (SEE APPENDIX B – PROGRAMS) FOR THE LIST OF AVAILABLE PROGRA M S,

THEIR SCREENS AND THE CHARACTERISTICS OF STERILIZABLE MATERIALS (IN RELATION
TO THE PROGRAMS).

NOTE

THE SELECTION CAN BE CHANGED AT ANY TIME BY FOLLOWING THE PROCEDURE

DESCRIBED ABOVE.

ACCESS TO A CUSTOM CYCLE DOES NOT REQUIRE A PASSWORD.
NONE OF THE COMBINATIONS AV AILA B LE IN THE CUSTOMIZATION PHASE CREATE ANY

RISKS OR DANGERS OF INJURY TO THE OPERATOR OR DAMAGE TOT HE DEVICE.

6. CONFIGURATION

28.

Setting the STAND-BY
mode

(STAND-BY OPTIONS on
the ADVANCED menu)

Based on the equipment's frequency of use, or other considerations, users may want to select
a high or low heating level during the STAND-BY (preheating) phase. They may also want to
select a STAND-BY time-out mode that determines when the STAND-BY is deactivated.
When you select STAND-BY OPTIONS with the ↵ key, you access the following menu:

→ ST- BY MODE +

ST- BY TIME- OUT ↑
EXIT ↓

-

When you select STAND-BY MODE, an additional menu appears where you can set the
heating level:

→ OFF +

LOW ↑
HIGH ↓

EXIT -

Select HIGH (high preheating level) to reduce the wait time between one cycle and the next.
Select LOW (low preheating) for normal use, since the wait time will be relatively shorter, in

any case.
Select OFF (deactivate preheating) for occasional use. In this case, the wait time will be longer

(up to about 10-12 minutes for a "cold start").
Move using the + and – keys, and confirm with the ↵ key.

On the other hand, when the STAND-BY TIME-OUT option is selected, it is possible to set the
time for deactivating STAND-BY, i.e., how many minutes after the last cycle the heating
elements are turned off.
The following screen appears:

TIMEOUT: XXX min
+/- to set

↵ to enter
⇑ to exit

It is possible to set a value of between 0 and 300 minutes (in 30-minute increments), after
which the heating elements are turned off (a condition similar to STAND-BY OFF), avoiding
the useless consumption of electricity.

Set using the + and – key, and confirm with the ↵ key.

NOTE

THIS OPTION IS ALSO ACTIVE WITH STAND-BY OFF. HOWEVER, IN THIS CONDITION

THE TIMER VALUE HAS NO EFFECT SINCE THE HEATING ELEMENTS ARE TURNED OFF
ANYWAY AT THE END OF THE STERILIZATION PROGRAM.

WHEN ANY CYCLE SELECTION KEY (STERILIZATION OR TEST) IS PRESSED, OR THE

MACHINE IS TURNED OFF AND ON WITH THE MAIN SWITCH, THE ORIGINAL STAND-BY
MODE (HIGH OR LOW) IS IMMEDIATELY REACTIV AT ED.

6. CONFIGURATION

29.

Setting the printing
mode

(PRINT OPTIONS on the
ADVANCED menu)

Printer model 1

Printer model 2

When the sterilizer is equipped with a printer (optional on the Bravo17, but standard on the
Bravo17V and 21V) for recording sterilization program data, it is necessary to set the
parameters required for its proper operation.

1. Select PRINT OPTIONS using the ↵ key and the following menu appears:

→ PRINTER +

REPORT ↑
EXIT ↓

-

Select PRINTER to access the settings for the printer used, or REPORT to set the number
of copies to print and to reprint data from the last program executed.

a) Item PRINTER

The following screen appears:

→ OFF +

INTERNAL ↑
EXTERNAL ↓

EXIT -

Select OFF to deactivate the printing of data at the end of a sterilization (or test) cycle.
Select INTERNAL to enable the thermal printer set (option) inside the front of the

sterilizer. In this case, another menu opens:

→ TYPE 1 +

TYPE 2 ↑
EXIT ↓

-

Select Type 1 for the model 1 of the printer installed.
Select Type 2 for the model 2 of the printer installed.

If, on the other hand, you choose EXTERNAL, the data will be printed on an external
peripheral. Following this selection, another menu opens:

→ CR TYPE +

CR+LF TYPE ↑
CR (+FF) TYPE ↓

CR+LF (+FF) TYPE –
EXIT

Activate CR to use printers that advance the paper only on the CR (Carriage Return)
command, or CR+LF for those that require the CR+LF (Carriage Return + Line Feed)
commands, or with +FF (Form-Feed) for printers that require the addition of this
command.

NOTE

CONSULT THE PRINTER MANUAL TO DETERMINE THE TYPE OF COMMAND USED. IF THIS

INFORMATION IS NOT AVAILABLE, TRY PRINTING WITH THE VARIOUS OPTIONS TO
IDENTIFY THE CORRECT SETTING.

6. CONFIGURATION

30.

b) Item REPORT

The following screen appears:

→ PRINTOUT MODE +

NR. COPIES ↑
PRINT LAST ↓

EXIT -

Select item PRINTOUT MODE to choose the mode in which the data is printed: The
following options appear:

→ AT CYCLE END +

STEP BY STEP ↑
EXIT ↓

-

Select AT CYCLE END to print the report at the end of the cycle.
Select STEP BY STEP to print the data at each phase of the cycle (see Examples of
printed report in Appendix B).

NOTE

IT IS NOT POSSIBLE TO MAKE MULTIPLE COPIES OF REPORTS IN STEP BY STEP MODE.
THE VACUUM AND BOWIE & DICK TEST REPORT WILL ONLY PRINT OUT AT CYCLE

END MODE.

Activate NR. COPIES to set the number of cycle report copies to print at the end of the
program. The following text appears:

COPIES: XX
+/- to set

↵ to enter
⇑ to exit

Set the number of copies desired (up to a maximum of 5). Confirm with the ↵ key.
To print a report from the last cycle executed (whether it terminated correctly or was

interrupted by an alarm), select PRINT LAST . The following screen will appear:

→ NORMAL PRINT +

EXTENDED PRINT ↑
EXIT ↓

-

The NORMAL PRINT command activates normal printing (showing relevant cycle
data and produced at the end of a correctly executed cycle), while EXTENDED PRINT
activates a more complete print out (including all the data typical of a cycle interrupted
by an alarm).

6. CONFIGURATION

31.

NOTE

IF THE LAST CYCLE ENDED CORRECTLY OR WAS INTERRUPTED BY MANUAL STOP, IT

IS POSSIBLE TO REPRINT THE REPORT IN EITHER NORMAL OR EXTENDED MODE. IF,
HOWEVER, THE LAST CYCLE WAS INTERRUPTED BY AN ERROR AND CORRESPONDING
ALARM, ONLY THE EXTENDED REPORT WILL BE AVAILABLE. THIS WILL FACILITATE
LATER TROUBLESHOOTING.

When selecting the reprint command, this message will be displayed:

NOW PRINTING
THE REPORT

PLEASE WAIT...

It will remain on the screen until the printing is complete.

Setting the tank filling
mode

(FILLING OPTIONS on
the ADVANCED menu)

The internal tank can be filled either manually or automatically. Automatic filling would occur
from an external device (container or demineralizer) connected to the Bravo - see Chapter 4 -
Installation).

Select FILL OPTIONS and the following menu appears:

→ AUTOMAT. FILLING +

MANUAL FILLING ↑
EXIT ↓

-

When AUTOMATIC FILL is selected, the unit will automatically fill the internal tank until the
maximum level (MAX signal) is reached and the MAX icon is displayed.

NOTE

ONLY ACTIVATE THE AUTOMATIC FILLING MODE AFTER THE EXTERNAL TANK HAS BEEN

FILLED WITH HIGH QUALITY DISTILLED WATER OR DEMINERALIZER. ALSO REMEMBER TO
OPEN THE TAP ON THE EXTERNAL TANK OR DEMINIERALIZER, IF REQUIRED.

When MANUAL FILL is selected, the internal tank must be filled manually (see Chapter 5 –
Instructions for Use).

To scroll through the items, use the + and - keys, and make a selection with the ↵ key.

Setting the
water draining mode

(DRAIN OPTIONS from
the ADVANCED menu)

The water used for the sterilization cycle can be drained into either the internal tank
(standard configuration) or the external SciCan tank of greater capacity (offered as an option
– see Chapter 4 - Installation) so as to reduce the frequency of emptying the used water.

Select DRAIN OPTIONS and the following menu appears:

→ INTERNAL DRAIN +

EXTERNAL DRAIN ↑
EXIT ↓

-

6. CONFIGURATION

32. .

Selecting INTERNAL DRAIN enables the reading of the MAX level sensor in the internal tank.
This is the setting that should be selected if connected directly to the drain.

Selecting EXTERNAL DRAIN enables the MAX level sensor located in the external tank and
in the internal tank.

NOTE

THE LEVEL SENSOR IN THE INTERNAL TANK REMAINS ACTI V E IN EITHER MODE TO

PREVENT A POSSIBLE MALFUNCTION OF THE EXTERNAL TANK OR A MISSING OR FAULTY
CONNECTION OF THE OPTIONAL EXTERNAL DRAIN TANK.

IF THE INSTALLATION HAS CONNECTED DIRECTLY TO THE DRAIN,
SELECT INTERNAL DRAIN.

To scroll through the items, use the + and - keys, and make a selection with the ↵ key.

Acquisition of the
ambient pressure

(AMBIENT PRESSURE
on the SPECIAL menu)

The first time the sterilizer is used and after any reinstallation, the sterilizer must acquire the
ambient pressure. This operation is necessary for the correct operation of several of the
device's auxiliary systems.
When AMBIENT PRESSURE is activated, the following screen appears:

ACQUISITION OF THE
AMBIENT PRESSURE

↵ to enter
⇑ to exit

NOTE

CHECK THAT THE STERILIZER DOOR IS COMPLETELY OPEN. IF YOU TRY TO ACQUIRE

THE PRESSURE WITH THE DOOR CLOSED THE FOLLOWING MESSAGE WILL BE DISPLAYED:

OPEN THE DOOR
TO CONTINUE

and will remain until the door is opened.
Confirm the acquisition of the data by pressing the ↵ key. This message appears:

PRESSURE VALUE
SET INTO MEMORY

accompanied by a beep to say that the ambient data pressure has been acquired.
Press the ⇑ key to cancel the operation.

6. CONFIGURATION

33.

Adjusting the
contrast of the liquid
crystal display

(LCD CONTRAST on the
SPECIAL menu)

The LCD contrast function adjusts the screens’ readability to compensate for the sterilizer
location’s lighting.

When LCD CONTRAST is activated, this screen appears:

ADJUSTMENT OF THE
LCD CONTRAST
+/- to set

⇑ to exit

Press the + key to increase the contrast and the - key to reduce it.
Adjust the contrast until the display is as clear and readable as possible, based on the

location’s normal conditions.

EXIT THE
CONFIGURATION
MODE

When you have completed the sterilizer configuration, return to the normal mode by selecting
EXIT and confirming with the ↵ key.
– This text will appear on the display:

BRAVO17
SETUP COMPLETE

↵ to exit
⇑ to resume

After several seconds, the device returns to normal operation in STAND-BY mode.

NOTE

TO RETURN TO THE FIRST LEVEL FROM ANY MENU, JUST SELECT EXIT AND CONFIRM

WITH THE ↵ KEY. YOU CAN ALSO PRESS ⇑ (ESC) KEY ONE OR MORE TIMES.

7. PREPARING THE MATERIAL
FOR STERILIZATION

34. .

7. PREPARING
MATERIAL FOR
STERILIZATION

Clean and rinse all instruments before loading them into the sterilizer. Disinfectant residues
and solid debris may inhibit sterilization and damage the instruments and the Bravo.

Unwrapped instruments, once exposed to ambient or external conditions, cannot be
maintained in a sterile state. If sterile storage is desired, wrap the instruments to be sterilized
according to the instrument manufacturer’s instructions, select the appropriate wrapped cycle
and allow it to run to completion.

NOTE

USER SHOULD USE ONLY STERILIZATION WRAPS THAT HAVE BEEN CLEARED FOR THEIR

MARKET. FOR U.S. CUSTOMERS, USE ONLY STERILIZATION WRAPS THAT HAVE BEEN
CLEARED BY FDA FOR THE STERILIZATION PROGRAM CHOSEN.

To promote drying and enable effective sterilization, wrapped or pouched instruments must not
touch each other.

SciCan recommends the final user carefully choose the most appropriate sterilization cycle
according to the recommendations of their leading infection control authorities and local
regulatory guidelines / recommendations.

WARNING

PLEASE REFER TO THE APPENDIX B - PROGRAMS (Introduction) FOR
THE LIST OF COMPATIBLE MATERIALS WITH THE STERILIZER.

TREATING TEXTILE
MATERIAL
BEFORE
STERILIZATION

With regards to textile material (or porous materials in general), such as smocks, napkins,
caps and other, carefully wash and then dry these before they are treated in the autoclave.

NOTE

DO NOT USE DETERGENTS WITH A HIGH CONTENT OF CHLORINE AND/OR PHOSPHATES.
DO NOT BLEACH WITH CHLORINE-BASED PRODUCTS. THESE SUBSTANCES CAN DAMAGE

THE TRAY SUPPORTS, TRA YS AND ANY M ETA L INSTRUMENTS THAT MAY BE PRESENT IN
THE STERILIZATION CHA MBER.

ARRANGING THE
LOAD

To ensure proper sterilization and to reduce wear on instruments, follow the instructions
below:

General notes for positioning on trays.

– Arrange instruments made of different metals (stainless steel, tempered steel, aluminum,

etc.) on different trays or keep them well separated from each other.

– For instruments not made of stainless steel, place a paper sterilization napkin or a muslin

cloth between the tray and the tool to avoid direct contact between these two different
materials.

– Always arrange objects with some distance between them and so that they will remain so

for the entire sterilization cycle.

– Make sure that hinged instruments are sterilized in an open position.
– Position cutting instruments, (scissors, scalpels, etc.) such that they do not come into

contact with each other during sterilization; if necessary, use a cotton or gauze cloth to
isolate and protect them.

– Arrange receptacles (glasses, cups, test tubes, etc.) on their sides, or upside down to

avoid pooling water.

– Do not load trays beyond their maximum indicated limit (see Appendix B).
– Do not stack trays or put them in direct contact with the walls of the sterilization chamber.
– Always use the tray support provided.
– To insert and remove trays from the sterilization chamber, always use the extractor

provided.

OK

OK

7. PREPARING THE MATERIAL
FOR STERILIZATION

35.

–

NOTE

PROCESS THE APPROPRIATE BIOLOGICAL/CHEMICALINDICATOR WITH EVERY TRAY TO

CONFIRM STERILIZATION HAS OCCURRED. IF PROCESSING WRAPPED MATERIAL, PL A CE
THE INDICATOR INSIDE ONE OF THE WRAPPINGS.

THE CUSTOMER SHOULD USE ONLY BIOLOGICAL INDICATORS THAT HAVE BEEN CLEARED

IN THEIR MARKET. FOR U.S. CUSTOMERS, ONLY USE BIOLOGICAL INDICATORS THAT
HAVE BEEN CLEARED BY FDA FOR THE STERILIZATION PROGRAM CHOSEN

Notes for rubber and plastic tubing

– Always rinse tubing with clean water before use and do not dry them.
– Arrange the tubing on the tray so that their ends are not obstructed or crushed.
– Do not bend or wind tubes, but allow them to lie as straight as possible.

Notes for packets and packages

– Arrange packages side-by-side, evenly spaced and not piled, and do not allow them to

come into contact with the walls of the chamber.

– When it is necessary to wrap an object, always use suitably porous material (sterilization

paper, muslin napkins, etc.) and close the wrapping with autoclave adhesive tape.

Notes for wrapped material

– It is best to wrap instruments individually, but if more than one instrument is placed in the

same envelope, make sure that they are made of the same metal;
– Seal the wrapping with adhesive tape designed for autoclaves or heat-sealing machines.
– Do not use staples, pins or other fasteners since they can compromise the maintenance of

sterility.
– Arrange the envelopes to avoid forming air pockets that obstruct the correct penetration

and removal of the steam.
– Orient the envelopes with the plastic side up and the paper side down.
– Always check that envelopes are correctly positioned and turn them over if necessary.
– If possible, place the envelopes on their sides using a suitable support.
– If pouched or wrapped loads are not dry when they are removed from the chamber, the

instruments must be used immediately or resterilized.

WARNING

IF YOU EXPECT TO STORE INSTRUMENTS, AL WA YS WRAP THEM. SEE
THE CHAPTER 10 – STORING STERILIZED MAT ERIAL.
THE USER SHOULD USE ONLY STERILIZATION WRAPS THAT HAVE
BEEN CLEARED FOR THEIR MARKET. FOR U.S. CUSTOMERS, ONLY
USE STERILIZATION WRAPS THAT HAVE BEEN CLEARED BY FDA FOR
THE STERILIZATION PROGRAM CHOSEN.

STERILIZATION
MONITORING

Chemical process monitors suitable for steam sterilizers at the indicated cycle temperatures
and times should be included in or on each package or load being sterilized. In addition,
SciCan recommends the use of biological monitors such as the EZTEST-STEAM indicator or
the 3M Attest system for routine monitoring of the sterilizer. It is important to select the correct
biological indicator for the cycle being tested.

OK

OK

8. PROGRAM SELECTION

36. .

8. PROGRAM
SELECTION

INTRODUCTION

Program selection is key to a successful sterilization process.
Since objects for sterilization can vary in shape, consistency and properties, it is important to

identify the most suitable program for it. This will not only preserve its physical characteristics
(avoiding or, at any rate, limiting alterations) it will ensure the most effective sterilization.

NOTE

A GUIDE TO SELECTING THE MOST SUITABLE PROGRAM FOR DIFFERENT LOAD TYPES IS

PROVIDED IN APPENDIX B (PR O GR A MS ).

PROCEDURE

Power on the unit as described in the Chapter 5 – Instructions for Use.

NOTE

IF THE PASSWORD FUNCTION HAS BEEN ENABLED (SEE CHAPTER 6 - CONFIGURATION -
SETTING THE PASSWORD), YOU WILL BE ASKED TO ENTER IT:

INSERT PASSWORD

↵ to enter
⇑ to exit

Enter the password using the + and – keys and confirm with the ↵ key.
At this point, the display will not offer any active pre-selection. It is waiting for the user to select

a program.
Press the PROGRAM SELECTION key one or more times until you reach the desired

program (1, 2, 3 or 4, also shown on the upper left of the display).

NOTE

WHEN THE SELECTION KEY IS PRESSED, THE FIRST STERILIZATION PROGRAM SHOWN IS

THE ONE THAT WAS USED FOR THE LAST CYCLE EXECUTED.

The top two lines of the display show the description of the selected program and the type of
drying set. Below are the set-point values for the temperature (°C), pressure (bar) and time
(mm:ss) of the selected cycle. For example:

1 134 POROUS/WRAPPED

NORMAL DRYING

134.0 °C

2.10 bar 04:00

After a brief interval, the two lower lines of the display will change and show the present
temperature and pressure values of the chamber, with the current date and time.

1 134 POROUS/WRAPPED

NORMAL DRYING

101.0 °C 30/08/02

0.01 bar 18:13:05

To cancel this selection, press ESC ⇑ on the control panel.

8. PROGRAM SELECTION

37.

NOTE

IF NO STERILIZATION PROGRAM IS SELECTED, THE EQUIPMENT CANNOT START A

STERILIZATION CYCLE, AN D THE FOLLOWING MESSAGE WILL APPEAR, WITH A BEEP:

SELECT A PROGRAM
PLEASE...

WARNING

IF YOU USE A PROGRAM THAT IS INAPPROPRIATE FOR THE TYPE OF
MATERIAL TO BE STERILIZED (SEE APPENDIX B) THE EFFECTIVENESS
OF THE STERILIZATION PROCESS IS NOT GUARANTEED.

9. RUNNING THE CYCLE

38. .

9. RUNNING
THE CYCLE

A sterilization cycle consists of a predetermined number of phases. Based on the type of air
extraction, sterilization process and drying method, the number and duration of these phases
can differ with each programs.

The electronic control system monitors the various phases, while checking that the various
parameters are respected. If any type of anomaly is encountered during the cycle, the program
is immediately interrupted, an alarm sounds and a code is displayed along with a message
explaining the nature of the problem.

STARTING THE
CYCLE

Password check

Printer paper-out check

If data recorder is
connected

After placing the load in the sterilization chamber, select the desired program and close the
door until you hear the click.

The door status icon will flash to indicate the door is closed.
Press the START button.

NOTE

IF THE PASSWORD FUNCTION HAS BEEN ENABLED (SEE CHAPTER 6 - CONFIGURATION -
SETTING THE PASSWORD), YOU WILL BE ASKED TO ENTER IT:

INSERT PASSWORD

↵ to enter
⇑ to exit

Enter the password using the + and – keys and confirm with the ↵ key.

The equipment will check for the presence of the paper in the on-board printer (if installed). If it
is out of paper the following message will be displayed:

WARNING

PAPER OUT

↵ to continue
⇑ to exit

Push key ↵ to bypass, but remember to replace the paper during or at the end of the cycle).
Push key ⇑ to return in Stand-by mode.

The unit will may check for the presence of a data recording device or depending on the type
of the device, the presence of a memory card inserted. If not plugged in, the display may
shows:

WARNING

CARD MISSING

↵ to continue
⇑ to exit

Ensure the data logger is properly connected and the proper memory card is installed then
press the key ↵ on the command panel.
Push the key ⇑ to interrupt the start command and return in Stand-by mode.

9. RUNNING THE CYCLE

39.

Door locking

If there is insufficient memory to store the new cycle data, the following message will be
displayed:

WARNING

CARD FULL

↵ to continue
⇑ to exit

Push key ↵ to continue without recording the cycle data.
Push key ⇑ to interrupt the start command; download the files onto a PC and delete the
memory content according to the instructions of the data recorder operating manual.
Repeat the Start command.

The unit locks the door.

When the door status icon

appears without blinking, the door is locked

When START is pushed, and for the entire sterilization cycle, the lower lines of the display will
show the following parameters:

Pressure of the sterilization chamber (bar)
Temperature of the sterilization chamber (°C)
Progressive time of the sterilization cycle (mm:ss)

1 134 POROUS/WRAPPED

WARMUP

101.9 °C

0.01 bar 00:00

Cycle time is counted from the start of the sterilization cycle (at the first vacuum phase), and
excludes the preheating phase.

PROGRAM
EXECUTION

Preheating

What follows is a phase by phase explanation of the execution of a sterilization cycle, using as
an example, the most complete and important cycle, the 134 POROUS/WRAPPED program.
This cycle is characterized by a fractionated pre-vacuum.

When the ST ART button is pressed, the first phase is PREHEATING, which brings the
chamber to the required temperature for the start of the cycle. The display shows the following:

1 134 POROUS/ WRAPPED

WARMUP

23.9 °C

0.01 bar 00:00

The icon that shows the status of the sterilization process is off.

or

MEMORY FULL

9. RUNNING THE CYCLE

40. .

First vacuum phase

First rise in
pressure

Second vacuum phase

Second rise in
pressure

Third vacuum phase

When the optimum temperature is reached, the first vacuum phase (1st VACUUM PULSE)
begins and the unit brings the chamber pressure down to the target value. The display shows:

1 134 POROUS/ WRAPPED

1. VACUUM PULSE

84.1 °C

- 0.69 bar 01:25

When the pre-set vacuum value is reached, steam is injected and the pressure begins to rise
(1st PRESSURE PULSE), until the target value is reached.

1 134 POROUS/WRAPPED

1. PRESSURE PULSE

108.0 °C

0.47 bar 03:58

At the end of the pressure rise, the steam, mixed with residual air, is discharged and the
second emptying of the sterilization chamber begins (2nd VACUUM PULSE).

1 134 POROUS/ WRAPPED

2. VACUUM PULSE

93.3 °C

- 0.79 bar 06:06

After the second vacuum phase, steam is again injected into the sterilization chamber, with a
corresponding rise in pressure (2nd PRESSURE PULSE).

1 134 POROUS/ WRAPPED

2. PRESSURE PULSE

11.4 °C

0.72 bar 07:44

The icon that shows the status of the sterilization process is always off.

At the end of the second pressure rise, there is another discharge and the last vacuum phase
begins (3rd VACUUM PULSE).

1 134 POROUS/ WRAPPED

3. VACUUM PULSE

89.9 °C

- 0.80 bar 09:52

9. RUNNING THE CYCLE

41.

Third rise in
pressure

Thermodynamic
equilibrium

Sterilization
time

Steam discharge

After the last vacuum phase, the pressure in the sterilization chamber must rise to the value
set for the sterilization process (3rd PRESSURE PULSE), always through the injection of
steam.

1 134 POROUS/ WRAPPED

3. PRESSURE PULSE

128.6 °C

1.70 bar 12:33

When the pressure and temperature values for the selected program have been reached, the
unit pauses to allow the temperature in the chamber to stabilize (EQUILIBRATION). The liquid
crystal display shows:

1 134 POROUS/ WRAPPED

EQUILIBRATION

135.4 °C

2.15 bar 13:40

When the thermodynamic parameters are balanced, the actual sterilization phase of the
materials begins (HOLDING TIME).
With continuous monitoring of the thermodynamic parameters and ongoing management of
the plumbing circuit, the pressure and temperature are remain constant within the limits
required by the program. A sterilization time countdown begins, and the display shows the
following:

1 134 POROUS/ WRAPPED

HOLDING TIME

135.6 °C 04:00

2.16 bar 13:55

The icon for the sterilization process status flashes to indicate that the treatment of the
load is in progress.

At the end of the sterilization phase, the icon

stays on to indicate the complete

sterilization of the material in the sterilization chamber.

WARNING

IF THE STERILIZATION CYCLE IS INTERRUPTED BEFORE COMPLETION,
THE ICON WILL CONTINUE TO FLASH. WHEN THIS HAPPENS, THE
MATERIAL CANNOT BE CONSIDERED STERILE AND MUST NOT BE
USED.

At the end of the sterilization phase, the steam is released from the sterilization chamber
(STEAM DISCHARGE). The liquid crystal display shows:

1 134 POROUS/ WRAPPED

DEPRESSURIZATION

123.9 °C

1.24 bar 18:20

The icon for the sterilization process status stays on.

countdown

9. RUNNING THE CYCLE

42. .

Drying

Ventilation

Leveling to the
atmospheric pressure

Completion
of the cycle

After the steam under pressure is released, the vacuum pump turns on to begin the drying
phase (DRYING). This creates a low pressure in the sterilization chamber to facilitate the
evaporation and consequent elimination of the steam. Depending on the type of drying
selected, one of the following screens will appear:

1 134 POROUS/ WRAPPED

DRYING (NOR)

101.1 °C

0.00 bar 18:51

1 134 POROUS/ WRAPPED

DRYING (INT)

101.1 °C

0.00 bar 18:51

1 134 POROUS/ WRAPPED

DRYING (+XX)

101.1 °C

0.00 bar 18:51

When the drying phase is complete, it is followed by a VENTILATION phase in which sterile,
fresh air is injected, while maintaining a vacuum in the chamber, to eliminate condensate and
cool the load.

1 134 POROUS/ WRAPPED

VENTILATION

84.4 °C

- 0.77 bar 26:51

At the end of the ventilation phase, the chamber is brought back to atmospheric pressure
(LEVELLING) by injecting sterile outside air to allow the opening of the door and the retrieval
of the load.

1 134 POROUS/ WRAPPED

LEVELLING

86.9 °C

- 0.43 bar 29:21

When the drying cycle is completed and the chamber pressure returns to pre-set safety limits,
the door status indicator will flash, the unit will beep and the door will unlock.

1 134 POROUS/ WRAPPED

CYCLE COMPLETE

86.2 °C

- 0.02 bar 29:40

The icon for the sterilization process status stays on.

Standard drying

Intelligent drying

EXTRA DRYING
(+XX) is the time
set

9. RUNNING THE CYCLE

43.

Open the door

Report print
(option)

Equipment ready

NOTE

AT THE END OF THE CYCLE, AND UP TO THE OPENING OF THE DOOR, THE HEATING

ELEMENTS ARE OFF TO ALLOW COOLING OF THE LOAD. ONLY AFTER THE LOA D HAS
BEEN REMOVED WILL THE UNIT RETURN TO ANY STAND-BY PREHEATING OPTIONS YOU
HAVE SELECTED.

NOTE

WHEN THE STERILIZER'S DOOR IS NOT OPENED AT THE END OF THE CYCLE, THE VACUUM

PUMP IS PERIODICALLY ACTIVATED TO REMOVE ANY TRACES OF CONDENSATE FROM THE
STERILIZATION CHAMBER. THE DISPLAY SHOWS:

FORCED VENTILATION

⇑ to stop

35.2 °C

- 0.02 bar 29:40

Press ⇑ to interrupt ventilation and open the door.

Open the door and retrieve the sterilized material, using the extractor provided.

When the door is opened, the icon

symbol turns off and the device goes to STAND-BY

mode as previously set.

When the door is opened, the report for the sterilization cycle executed is automatically
produced (if the printer or data logger is installed). Refer to the print report examples shown in
Appendix B, Programs.

If a data logger is installed, never remove the USB stick until the report is fully downloaded,
which is indicated by a quick flashing light on the USB stick and a message on the LCD
display.

NOTE

IF THE PRINTOUT STEP BY STEP OPTION IS SELECTED, THE REPORT WILL BE PRINTED

AT THE COMPLETION OF E A CH PHASE OF THE CYCLE.

The device is ready to execute a new cycle.
Repeat the procedures explained in the Chapter 8 - Program Selection to execute a new
sterilization cycle.

RESULT OF THE
CYCLE

After the cycle is finished, it is important to check the sterilization results.
The report (option) of the sterilization parameters is an additional verification tool.

9. RUNNING THE CYCLE

44. .

CHECKING THE
CYCLE DATA
REPORT (FOR
UNITS WITH
PRINTERS)

It is a good practice to check that the print report issued at the end of the sterilization program,
also specifies a positive outcome.

At the end of the cycle, the relevant data for the thermodynamic parameters of the sterilization,
i.e., temperature and pressure (°C and bar), and time (in minutes) of the sterilization cycle,
along with particular attention to the sterilization phase, will print automatically when the door
is opened.

Check the values on the print report and any additional indications for further confirmation of
sterilization.

The operator should sign in the space provided and file the document for possible future use.
If necessary, copies of the document can be used to identify the load (or parts of it) with the

date/time of sterilization and details of the type of cycle performed.

To select the number of copies to print, consult Chapter 6 - Configuration.

NOTE

THE OPERATOR CAN ALSO REQUEST AN EXTENDED PRINTOUT OF THE STERILIZATION

PROCESS DATA, INCLUDING THE RECORDED VALUES OF ALL THE SENSORS INSTALLED
ON THE MACHINE. TO START THIS PRINT FUNCTION, HOLD DOWN THE ⇑ (ESC) KEY ON
THE CONTROL PANEL WHILE OPENING THE DOOR.

FOR COMPLETE DETAILS ABOUT PRINTING THE SUMMARY, PLEASE REFER TO THE

REPORT EXAMPLES SHOWN IN APPENDIX B, PROGRAMS.

MANUAL CYCLE
INTERRUPTION

The operator can manually interrupt the cycle at any time by pressing the START/STOP key
for three seconds. This command generates the error E999, because the cycle did not finish
correctly. Until it is safe to open the door, the unit will beep and the display will show:

MANUAL STOP
LEVELLING...

101.2 °C E999

- 0.47 bar 26:01

When safe conditions are reached, the machine activates a special procedure, first asking the
user to manually unlock the door by displaying the following instruction:

PRESS ⇑ TO
UNLOCK THE DOOR

86.2°C E999

- 0.02 bar 26:01

Press the ⇑ key to unlock the door.
The following message is then displayed:

MANUAL STOP
OPEN THE DOOR

85.8°C E999

- 0.01 bar 26:01

> 3s

Error code

9. RUNNING THE CYCLE

45.

RESETTING THE
SYSTEM

Finally, when the door is opened, you will be asked to reset the device by the following
message:

MANUAL STOP
RESET SYSTEM

85.5°C E999

- 0.01 bar 26:01

To RESET the system, press and hold the PROGRAM SELECTION key for at least three
seconds until you hear the confirmation beep.

When the door is opened, the report for the sterilization cycle executed is produced, including
the error code (E999). Check the report, initial it in the space provided and file it in a suitable
place.
For more information, refer to the print report examples shown in Appendix B, Programs.

After the RESET, the device goes into STAND -BY mode, ready to execute a new program.

NOTE

WHEN AN ALARM IS GENERATED AT CERTAIN PHASES OF THE C YCLE, AN AUTOMATIC

PROCEDURE IS ACTIVATED TO CLEAN THE PLUMBING CIRCUIT. FOR A COMPLETE
DESCRIPTION OF THE ALARMS , SEE APPENDIX E - ALARMS .

NOTE

AFTER AN ABORTED CYCLE, DUE TO A BLACK-OUT OR A POWER FAILURE, THE USER
CANNOT ACCESS THE CHAMBER UNTIL TO THE POWER RETURNS.
AT THAT TIME, THE USER MUST RESET THE UNIT ACCORDING TO THE PROCEDURE

DESCRIBED IN THE APPENDIX E – ALAR M S (ALARM INTERVENTION).

AT THE START OF THE NEXT CYCLE, AN AUTOMATIC PROCEDURE IS ACTIVATED TO

CLEAN THE PLUMBING CIRCUIT. FOR A COMPLETE DESCRIPTION OF THE ALARMS, SEE

APPENDIX E - ALARM S.

WARNING

IF THE ICON IS OFF, THE MATERIAL IN THE STERILIZATION
CHAMBER CANNOT BE CONSIDERED STERILE AND MUST NOT BE
USED.

> 3s

10. STORING STERILIZED MATERIALS

46. .

10. STORING
STERILIZED
M AT E R I AL S

INTRODUCTION

The sterilized material must be adequately treated and stored to maintain its sterility over time,
until its use.

Inadequate storage can cause rapid recontamination.
This leads to problems regardless of what you do since you will either be using

recontaminated material (most of the time unconsciously), placing the user and patient at risk,
or you will have to run the sterilization cycle again, with an inevitable waste of time and
resources.

For this reason, we think it will be useful to provide several basic suggestions, leaving the
operator the task of further study of specific texts.

HANDLING

Assuming that the sterilizer is located in a clean place, free of dust and not too damp, the
following precautions should be taken when handling and/or carrying sterile material:

1. Remove the load from the sterilization chamber wearing gloves and a clean, or even
better, sterilized smock. As an additional precaution, wear a protective mask on your face;

2. Rest the tray on a dry, suitably clean and disinfected surface. Take care to distance or, at
any rate, separate the sterile material from the area where contaminated material is kept
waiting to be sterilized;

3. Touch the material and/or instruments as little as possible, taking extreme care not to cut
or damage the wrappings;

4. Let the instruments cool before any transport (and subsequent storage). If necessary for
transport, transfer the material using dry, clean and disinfected containers. The containers
must be closed or, if open, covered with clean cloths.

STORAGE

Sterile material waiting for used must be stored using the appropriate techniques. These will
significantly slow recontamination:

1. Store the material and/or instruments in the protective wrappings that were used during
sterilization. Do not wrap the instruments after sterilization since, in addition to being
useless and completely senseless, is also potentially damaging;

2. Store the material in a dry, suitably clean and disinfected place, far from the area where
infected material passes. If possible, use closed compartments equipped with ultraviolet
light;

3. Identify the sterile material by attaching the sterilization data (attaching a copy of the
printed report or an adhesive label);

4. First use the material that has been stored the longest (FIFO, "First In First Out"). This
results in material that is homogeneously stored, avoiding storing for too long, with the
consequent risks.

5. Never store material for too long. In fact, do not overlook the fact that materials will tend to
degrade and be recontaminated in a finite time, even when the above instructions are
followed.

NOTE

UNPACKAGED INSTRUMENTS AND MATERIALS MUST BE STORED IN A CLOSED, DRY,
CLEAN AND DISINFECTED PL ACE, POSSIBLY EQUIPPED WITH ULTRAVIOLET LIGHT.

PLEASE REMEMBER THAT UNPACKAGED INSTRUMENTS AND /OR M A TE RIAL S ARE NOT

SUITABLE FOR LONG TIME STORAGE.

IT IS RECOMMENDED THEIR IMMEDIATE USE AFTER THE STERILIZATION PROCESS.

WARNING

CONSULT THE SPECIFICATIONS PROVIDED BY THE MANUFACTURER
OF THE PACKAGING MATERIAL FOR INFORMATION ON THE MAXIMUM
ALLOWED STORAGE TIME.

11. TEST PROGRAMS

47.

11. TEST
PROGRAMS

INTRODUCTION

The Bravo product line offers two test programs to periodically check the unit’s effectiveness.
The two programs are:

• BOWIE & DICK Test

• Vacuum Test

The BOWIE & DICK Test program executes a cycle at 134 °C for a duration of 3.5 min. This
cycle has a fractionated vacuum phase similar to that used in the POROUS and HOLLOW
programs. Using a suitable test pack, it is possible to evaluate the correct penetration of the
steam inside porous loads (see the following paragraph).

The Vacuum Test program tests the seal of the sterilizer's entire plumbing system. By
measuring the variation in the degree of vacuum in a certain span of time and comparing it
with pre-set limit values, it is possible to determine the effectiveness of the seal of the
sterilization chamber, the various tubes and the cut-off devices.

BOWIE & DICK
TEST

To select the BOWIE & DICK Test program, press the Test Selection key one or two times
until the display reads:

BOWIE & DICK TEST

134.0°C

2.15 bar 03:30

The test device is a Bowie & Dick test pack, manufactured according to the applicable
standards. To execute the test, insert the Bowie & Dick test pack in the chamber.

NOTE

THE DEVICE AND CHEMICAL INDICATORS FOR RUNNING THE BOWIE & DICK TEST

PROG R AM AR E NOT SUPPLIED WITH THE DEVICE. TO REQUEST INFORMATION IN THIS
REGARD, CONTACT SCICAN'S CUSTOMER SUPPORT DEPARTMENT (SEE APPENDIX Z).

Place the test pack horizontally on the device's lowest tray, in the front part of the chamber,
near the door. Do not put any other material inside the chamber.

Close the door and start the program by pressing the START key.

NOTE

IN ADDITION, THE UNIT CHECKS THE PRESENCE OF PRINTER PAPER (IF PRINTER

EQUIPPED) AN D, IF A DATA RECORDER IS CONNECTED, THE PRESENCE OF THE FL ASH
CARD AND ITS MEMORY CAPAC ITY.

THE POSSIBLE WARNING MESSAGES, AND THE CONSEQUENT ACTIONS TO CARRY OUT,

ARE THE SAME AS DESCRIBED FOR A STANDARD STERILIZATION CYCLE.

NOTE

FOLLOW THE INSTRUCTIONS PROVIDED BY THE INDICATOR'S MANUFACTURER FOR ITS
METHODS OF USE, INDICATION AND ANY OTHER TECHNICAL DETAILS.

As the door is opened at the end of the cycle, a report will be printed providing relevant data
for the test cycle performed (if the printer is installed).

For complete details about printing summaries, please refer to the report examples shown in
Appendix B, Programs.

11. TEST PROGRAMS

48. .

VACUUM TEST

To select the VACUUM TEST program, press the Test Selection key one or two times until
the display reads:

VACUUM TEST

- 0.80 bar

The Vacuum Test program is run with the sterilization chamber empty, except for the trays and
their supports.

NOTE

RUN THE VACUUM TEST AS THE FIRST CYCLE AFTER POWERING-ON THE EQUIPMENT.

To avoid the heating of the sterilization chamber influencing the variation of the vacuum value
measured during the Vacuum Test, the system is programmed to prevent running this test
when the temperature sensors of the sterilization chamber show a value higher than 50° C.

If you try to start the program with a higher temperature than indicated above, the display will
read:

WARNING!
PT1 OVERHEATING

- 0.80 bar

After a short time, the device will automatically return to STAND-BY mode, ready for use.

NOTE

TO RAPIDLY LOWER THE TEMPERATURE OF THE CHAMBER LEAVE THE STERILIZER'S

DOOR OPEN UNTIL THE CORRECT TEMPERATURE IS REACHED.

Close the door and start the program with the START key.

NOTE

IN ADDITION, THE EQUIPMENT CHECKS THE PRINTER PAPER PRESENCE (OPTION) AN D , IF

A DATA RECORDER IS CONNECTED, THE PRESENCE OF THE FLASH CARD AND ITS
MEM O RY C A PACI T Y.

THE POSSIBLE WARNING MESSAGES, AND THE CONSEQUENT ACTIONS TO CARRY OUT,

ARE THE SAME AS DESCRIBED FOR A STANDARD STERILIZATION CYCLE.

The vacuum phase will begin immediately and the display reads:

VACUUM TEST
VACUUM PULSE

- 0.69 bar 01:02

The display shows the pressure (bar), and the total time from the start of the program.
When the pre-set pressure is reached (-0.80 bar) the pump stops and the pressure

stabilization phase begins (WAITING PERIOD). This lasts 5 minutes is shown on the display:

11. TEST PROGRAMS

49.

VACUUM TEST
WAITING PERIOD
05:00

- 0.80 bar 01:48

During this phase, a variation of not more than 10% of the maximum low pressure is allowed.
Beyond this, the test will fail.

When the waiting phase is complete, the pressure verification phase begins (LEAKAGE
PERIOD). This will last 10 minutes:

VACUUM TEST
LEAKAGE PERIOD
10:00

- 0.79 bar 06:48

In this phase, a variation of up to ±0.02 bar is allowed, compared to the initial phase value.
Higher variations, however, will cause the test to fail.
The time is counted down until the phase is completed, after which the pressure is brought
back to atmospheric pressure.

VACUUM TEST
LEVELLING

- 0.29 bar 17:19

When the program finishes, the display will read:

VACUUM TEST
TEST PASSED

- 0.01 bar 17:44

The end of the program is signaled with a beep.

NOTE

IF THE PRESSURE CHANGE EXCEEDS THE PRE-SET LIMIT, THE PROGRAM IS INTERRUPTED

AND ALARM MESSAGE IS GENERATED.

SEE A COMPLETE DESCRIPTION OF THE ALARMS IN APPENDIX E .

When the door is opened at the end of the program, a report of the test cycle is printed (if the
printer is installed) with all the salient data.

For complete details about printed reports, please refer to the examples shown in Appendix
B, Programs.

APPENDIX A – TECHNICAL CHARACTERISTICS

50. .

APPENDIX A – TECHNICAL CHARACTERISTICS

SUMMARY TABLE

Device

Autoclave

Models

Bravo17, Bravo

17V

, Bravo

21V

Manufacturer

SciCan Ltd.

1440 Don Mills Road Phone: [phone]
Toronto ON M3B 3P9 Fax: [phone]
CANADA Toll free: 1-800-667-7733

Power supply (see identification
plate on the device)

120V, 60 Hz

220/230V, 60Hz

220/240V, 50Hz

Nominal power

1700 W (15A)

2300 W (10A)

2300 W (10A)

Mains fuses (6.3 x 32 mm)

F 15A

F 15A

F 15A

On-board

fuses

5 x 20 mm

F1 (Secondary trafo):
F2 (Primary trafo):
F3 (doorlock accidental
activation):
F4 (doorlock overload):
F1 PTR (printer protection):

T 5A 250V
T 4A 250V
F 200mA 250V

F 1.25A 250V
T 5A 250V

T 5A 250V
TT 2A 250V
F 200mA 250V

F 1.25A 250V
T 5A 250V

T 5A 250V
TT 2A 250V
F 200mA 250V

F 1.25A 250V
T 5A 250V

External dimensions (LxDxH)

(excluding rear connections)

Bravo17, Bravo

17V

: 480 x 560 x 420 mm / 18.9” x 22.04” x 16.5”

Bravo

21V

: 480 x 660 x 420 mm / 18.9” x 25.98” x 16.5”

Insulation class

Class I

Installation category

Cat. II

Environment of use

Internal use

Noise level

<60 db(A)

Environmental operating
conditions

Temperature Rating:: +15 °C to +40 °C
Relative humidity: max 80%, non-condensing
Altitude: max 3000 m (a.s.l.)

Net weights

Bravo17: ~ 50 kg / 110 lbs (empty)
~ 55 kg / 121 lbs (empty with trays and support)
~ 59 kg / 130 lbs (empty with trays, supports, MAX water

Bravo

17V

: ~ 53 kg / 117 lbs (empty)

~ 58 kg / 128 lbs (empty with trays and support)
~ 62 kg / 137 lbs (empty with trays, supports, MAX water)

Bravo

21V

: ~ 58 kg / 128 lbs (empty)

~ 63 kg / 139 lbs (empty with trays and support)
~ 67 kg / 148 lbs (empty with trays, supports, MAX water)

Sterilization chamber dimensions

(Diameter x Length)

Bravo17, Bravo

17V

: D250 x L343 mm / D10” x L13.5”

Bravo

21V

: D250 x L445 mm / D10 ” x L17.5”

Sterilization chamber total volume

Bravo17, Bravo

17V

: ~ 17 L (0.017 m3 / 0.60 ft3)

Bravo

21V

: ~ 21 L (0.021 m3 / 0.74 ft3)

Distilled water tank capacity

(supply)

~ 4.6 L / 1.22 US gal (water at MAX level)
~ 0.8 L / 0.02 US gal (water at MI N level)

Sterilization programs

Available: 10 (see Appendix B)
Pre-sets: 4 (direct selection by user)

Test programs

BOWIE & DICK Test, Vacuum Test

Preheating time (from cold)

~ 10 minutes

Serial connection

DB-9 pin (female) connector

Bacteriological filter

(PTFE filtering element)

Porosity: 0.2 µm
Connection: male 1/8" NPT connector

APPENDIX A – TECHNICAL CHARACTERISTICS

51.

SAFETY DEVICES

The sterilizer is equipped with the following safety devices:

– Mains fuses (see summary table data)

Protects inside the device against a fault in the heating elements.
Action: cuts the electricity.

– Fuses protecting the electronic circuits (see summary table data)

Protects against a fault in the primary transformer circuit and low voltage uses.
Action: cuts power to one or more low-voltage circuits.

– Thermal circuit breakers on the mains voltage windings

Protects against overheating of the vacuum pump motor and the primary transformer windings.
Action: temporary cut-off (until cooling) of the winding.

– Safety valve

Protects against overpressure in the sterilization chamber.
Action: releases the steam and restores to a safe pressure.

– Steam generator manual re-arm safety thermostat

Protects against steam generator overheating.
Action: cuts-off the electricity to the steam generator.

– Heating element manual re-arm safety thermostat

Protects against overheating of the heating elements of the container under pressure.
Action: cuts-off the electricity to the chamber heating element.

– Door position safety microswitch

Confirms the door is correctly closed when the container is under pressure.
Action: signals incorrect door position.

– Mechanized door lock mechanism with electromechanical protection (pressure switch)

Protects against accidental opening of the door (even in a blackout).
Action: locks the door.

– Door lock mechanism safety microswitch

Confirms the door lock is operating correctly.
Action: signals the failure or incorrect operation of the door lock mechanism.

– Self-leveling plumbing system

Plumbing system structure that allows for the spontaneous leveling of pressure in the case of a manual interruption of the
cycle, alarm or blackout.
Action: automatically restores atmospheric pressure in the sterilization chamber.

– Integrated system for evaluating the sterilization process

Provides continuous verification of the sterilization process parameters entirely managed by microprocessor.
Action: in case of anomaly, immediately interrupts the program and generates alarms.

– Monitoring of the sterilizer's operation

Provides real-time oversight of all significant parameters when the machine is on.
Action: in case of anomaly, generates alarm messages with possible interruption of the cycle.

APPENDIX A – TECHNICAL CHARACTERISTICS

52. .

WATER SUPPLY CHARACTERISTICS

DESCRIPTION

WATER SUPPLY VALUES

VALUES IN

CONDENSATE

DRY RESIDUE

< 10 mg/l

< 1 mg/l

SILICON OXIDE SiO2

< 1 mg/l

< 0.1 mg/l

IRON

< 0.2 mg/l

< 0.1 mg/l

CADMIUM

< 0.005 mg/l

< 0.005 mg/l

LEAD

< 0.05 mg/l

< 0.05 mg/l

HEAVY METAL RESIDUES
(except iron, cadmium and lead)

< 0.1 mg/l

< 0.1 mg/l

CHLORINES

< 2 mg/l

< 0.1 mg/l

PHOSPHATES

< 0.5 mg/l

< 0.1 mg/l

CONDUCTIVITY AT 20 °C

< 15 µs/cm

< 3 µs/cm

pH VALUE

5 - 7

5 - 7

APPEARANCE

colorless, transparent,

without sediments

colorless, transparent,

without sediments

HARDNESS

< 0.02 mmol/l

< 0.02 mmol/l

NOTE

WHEN PURCHASING DISTILLED WATER, ALWAYS CHECK THAT THE QUALITY AND CHARACTERISTICS

DECLARED BY THE PRODUCER ARE COMPATIBLE WITH THOSE SHOWN IN THE TABLE.

WARNING

THE USE OF WATER CONTAINING CONTAMINANTS IN LEVELS EXCEEDING THOSE

SHOWN IN THE TABLE WILL SIGNIFICANTLY SHORTEN THE STERILIZER'S LIFE.
IN ADDITION, THIS MAY INCREASE THE OXIDATION OF MORE SENSITIVE MATERIALS
AND INCREASE LIME RESIDUES ON THE GENERATOR, BOILER, INTERNAL SUPPORTS
AND INSTRUMENTS.

APPENDIX B – PROGRAMS

53.

APPENDIX B – P R OGR A MS

INTRODUCTION

The steam sterilizer is appropriate for almost all materials and instruments, so long as they are able to tolerate, without
damage, a minimum temperature of 121 °C.

The following material can typically be sterilized with steam:

– Stainless steel surgical/generic instruments;
– Carbon steel surgical/generic instruments;
– Rotating and/or vibrating instruments driven by compressed air (turbines) or mechanical transmission (counter-angles,

tooth scalers);
– Glass articles:
– Mineral-based articles;
– Articles made of heat-resistant plastic;
– Articles made of heat-resistant rubber;
– Heat-resistant textiles;
– Medical textiles (gauze, pads, etc.);

NOTE

TO PREVENT THE INSTRUMENTS AND/OR MATERIALS FROM ELECTROLYTHIC CORROSION DURING THE

STERILIZATION PROCESS, PLEASE AVOID DIRECT CONTACT BETWEEN THE FOLLOWING METALS:

ALUMINUM (AL) - NICKEL (NI);
CARBON STEEL – NICKEL (NI);
NICKEL (NI) – CHROME (CR);
COPPER (CU) – ALUMINUM (AL);
CARBON STEEL – COPPER (CU);
CHROME (CR) – COPPER (CU);
STAINLESS STEEL – ALUMINUM (AL);
CARBON STEEL – STAINLESS STEEL;
CHROME (CR) – STAINLESS STEEL.

ALWAYS SEPARATE THE INSTRUMENTS AND/OR MATERIALS BY METAL TYPE AND ELECTROLYTHIC COMPATIBILITY.

NOTE

DEPENDING ON THE CONFORMATION OF THE MATERIAL (SOLID, HOLLOW OR POROUS), ANY PACKAGING
(PAPER/PLASTIC ENVELOPE, STERILIZATION PAPER, CONTAINER, MUSLIN NAPKIN, ETC.) AN D ITS HEA T -

RESISTANCE, IT IS IMPORTANT THAT YOU CHOOSE THE APPROPRIATE PROGRAM BY REFERRING TO THE TABLE
SHOWN ON THE NEXT PAGE.

WARNING

THE DEVICE MUST NOT BE USED FOR STERILIZING FLUIDS, LIQUIDS OR PHARMACEUTICAL
PRODUCTS.

APPENDIX B – PROGRAMS

54. .

PROGRAM SUMMARY TABLE

PROGRAM

DESCRIPTION

N O M I N A L

V A L U E S

BASIC PROGRAM

PARAMETERS

STERILIZABLE MATERIAL

NOTES

Temperature

(°C)

Pressure

(bar)

Holding time

(min)

Pre-vacuum

(1)

(F=fractionated; S=single)

Standard drying

(2)

(L=long; S=short)

Total cycle time

(3)

(approx. max.)

Average consumption H

2

O

(ml/cycle)

Average energy consumption

(kWh/cycle)

TYPE

MAX TOTAL MASS

(kg)

MAX MASS

PER TRAY (kg)

MAX MASS

PER ARTICLE (kg)

220V

17

17V

21V

17/17V

21V

17/17V

21V

134 POROUS /
WRAPPED

134

2.10 4 F L 43’

38’

43’

525

0.8

Unpackaged
porous material

1.00

1.25

0.30

0.40

0.30

For material and

instruments in

(single and

double)

packaging, we

recommend

using the 3-tray

configuration

Porous material
in single package

0.75

1.00

0.25

0.30

0.25

Porous material
in double
package

0.60

0.75

0.20

0.25

0.20

Solid material /
handpieces in
single package

3.00

4.00

1.00

1.25

0.25

Solid material /
handpieces in
double package

1.50

2.00

0.50

0.60

0.25

121 POROUS /
WRAPPED

121

1.10

20 F L

58’

53’

58’

550

0.8

Unpackaged
porous material

1.00

1.25

0.30

0.40

0.30

Porous material
in single package

0.75

1.00

0.25

0.30

0.25

Porous material
in double
package

0.60

0.75

0.20

0.25

0.20

Solid material /
handpieces in
single package

3.00

4.00

1.00

1.25

0.25

Solid material /
handpieces in
double package

1.50

2.00

0.50

0.60

0.25

134 HOLLOW /
UNWRAPPED

134

2.10 4 F S 38’

31’

36’

525

0.7

Unpackaged
handpieces

6.00

7.50

1.20

1.50

0.50

121 HOLLOW /
UNWRAPPED

121

1.10

20 F S

53’

46’

51’

550

0.7

Unpackaged
handpieces

6.00

7.50

1.20

1.50

0.50

134 SOLID /
WRAPPED

134

2.10 4 S L 32’

26’

30’

300

0.6

Solid material in
single package

3.00

4.00

1.00

1.25

0.25

121 SOLID /
WRAPPED

121

1.10

20 S L

47’

41’

45’

325

0.6

Solid material in
single package

3.00

4.00

1.00

1.25

0.25

134 SOLID /
UNWRAPPED

134

2.10 4 S S 24’

21’

25’

300

0.5

Unpackaged
solid material

6.00

7.50

1.20

1.50

0.50

121 SOLID /
UNWRAPPED

121

1.10

20 S S

39’

36’

41’

325

0.5

Unpackaged
solid material

6.00

7.50

1.20

1.50

0.50

134 EMERGENCY

134

2.10 3 S S 16’

12’

14’

300

0.45

Unpackaged
solid material

0.50

0.50

0.50

0.50

0.50

134/121 CUSTOM

(4)

134

or

121

2.10
or

1.10

> 4

or

> 20

F/S

L/S

56’

max

48’

max

58’

max

550
max

0.9

max

Unpackaged
solid material

6.00
max

7.50

(ma x)

1.20
max

1.50
(ma

x)

0.50
max

HELIX /
BOWIE & DICK TEST

134

2.10

3.5 F S

22’

20’

22’ - -

Test pack only

(without any
other load)

- - - - -

VACUUM TEST

-

-0.80

-

-

-

22’

18’

18’ - -

Empty chamber

- - - - -

APPENDIX B – PROGRAMS

55.

GENERAL NOTES

(1) FRACTIONATED = Pre-vacuum stage completed with a sequence of 3 vacuum pulses + 3 pressure pulses.

“Fractionated vacuum” programs are dedicated to the sterilization of porous materials or handpieces.
SINGLE = Pre-vacuum stage completed by 1 vacuum + 1 pressure pulse.

“Single vacuum” programs are dedicated to the sterilization of solid materials.

(2) LONG = Drying stage for porous material and/or handpieces and/or solid material in single/double package.

The validated LONG drying time (STANDARD option) is 16.5 min.
The EXTRA and INTELLIGENT options have not been validated.
SHORT = Drying stage for unpackaged solid instruments and/or unpackaged handpieces.

The validated SHORT drying time (STANDARD option) is 7 min.
The FAST option, with a drying time of 2.5 min (up to a load of 1.0 kg max) has not been validated.

(3) The Total Cycle Time indicates the approximate time required for the completion of the entire program. It

does not include warm up phase initiated when the start button is pressed. Times are dependant on input
voltage and load condition.

(4) The program 121°C / 134°C CUSTOM has holding times of 20 minutes (or more) and 4 minutes (or more)

respectively at 121°C and 134°C.
Pre-vacuum type and D r y i n g t y p e can be set according to the indications given in the notes (1) and (2)

above.

The 121°C / 134°C CUSTOM programs have not been validated.

APPENDIX B – PROGRAMS

56. .

STERILIZATION PROGRAM DIAGRAM

APPENDIX B – PROGRAMS

57.

APPENDIX B – PROGRAMS

58. .

APPENDIX B – PROGRAMS

59.

APPENDIX B – PROGRAMS

60. .

APPENDIX B – PROGRAMS

61.

DIAGRAMS OF THE TEST CYCLES

APPENDIX B – PROGRAMS

62. .

EXAMPLES OF PRINTED REPORTS

Cycle Report (normal)

Model Bravo17
S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0007/0015
Selection 134c SOLID/UNWRAPPED
Temperature 134 °C
Pressure 2.10 bar
Process time 4 m i n
Stand-by L O W
Pre-vacuum SINGLE
Drying FAST

CYCLE START 19/11/02
12:14

T i m e C bar

---------------------------------------------------------­00:01 CS 079.4 +0.00
02:02 1PV 093.7 -0.80
05:48 ET 135.6 +2.15
06:02 SS 135.9 +2.17
07:02 135.6 +2.14
08:02 135.5 +2.14
09:02 135.4 +2.14
10:02 SE 135.5 +2.15
10:37 DS 104.1 +0.00
11:41 SPD 047.5 -0.90
16:08 DE 047.6 -0.84
17:12 CE 084.6 -0.04

06:32 MAX 136.0
09:59 MIN 135.4

Drying PuIses 01
CYCLE END 19/11/02
12:27

STERILIZATION: POSITIVE

OPERATOR

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

---------------------------------------------------------­Model Bravo17

S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0007/0015
Selection 134c POROUS/WRAPPED
Temperature 134 °C
Pressure 2.10 bar
Process time 4 m i n
Stand-by HIGH
Pre-vacuum FRACTIONATED
Drying STANDARD

CYCLE START 19/11/02
09:52

T i m e C bar

---------------------------------------------------------­00:01 CS 075.1 -0.00
01:57 1PV 047.S -0.80
04:53 1PP 120.5 +1.00
07:00 2PV 061.1 -0.80
09:15 2PP 120.4 +0.98
11:22 3PV 061.1 -0.80
15:04 ET 135.5 +2.15
15:19 SS 135.9 +2.17
16:19 135.4 +2.14
17:18 135.5 +2.15
18:19 135.4 +2.14
19:19 SE 135.5 +2.15
19:53 DS 104.4 +0.00
20:57 SPD 048.4 -0.90
26:55 EPD 094.9 -0.86
29:15 DE 112.6 -0.47
29:43 CE 115.8 -0.04

16:20 MAX 135.9
18:11 MIN 135.4

Drying Pulses 05
CYCLE END 19/11/02
10:17

STERILIZATION: POSITIVE

OPERATOR

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Cycle Report (extended)

at the operator's request

Model Bravo17
S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0007/0015
Selection 134c POROUS/WRAPPED
Temperature 134 °C
Pressure 2.10 Bar
Process time 4 m i n
Stand-by HIGH
Pre-vacuum FRACTIONATED
Drying STANDARD

CYCLE START 19/11/02
09:52

T i m e T1 P T2 T3 T4

------------------------------------------------------------------­00:01 CS 075.1 -0.00 130.9 115.2 093.4
00:11 074.9 -0.28 133.3 114.2 094.0
00:21 074.4 -0.46 146.3 113.2 094.5
00:31 074.3 -0.57 152.6 112.2 095.0
00:35 .. 074.3 -0.59 154.2 111.9 095.2
00:51 .. 078.9 -0.62 152.2 110.4 095.6
01:01 .. 074.9 -0.73 146.6 109.6 095.7
01:27 .. 047.8 -0.78 149.3 107.7 095.7
01:57 .. 047.8 -0.80 155.3 105.8 095.4

02:07 .. 076.5 -0.57 149.9 105.2 095.1
02:17 .. 081.1 -0.49 142.1 104.6 094.6
……………
……………
08:15 … 068.4 -0.76 151.8 104.7 102.3
08:22 … 061.1 -0.80 153.6 104.5 101.7

08:32 ... 097.4 +0.01 154.7 104.0 100.8
08:42 … 104.6 +0.24 148.9 103.7 101.0
……………
……………
15:04 … 135.5 +2.15 143.3 111.7 131.7

15:19 … 135.9 +2.17 148.5 113.5 132.6
15:28 … 135.3 +2.16 153.6 115.9 133.0
……………
……………
19:19 … 135.5 +2.15 157.4 126.5 132.5

19:34 … 134.4 +1.07 157.0 126.8 131.2
19:49 … 108.3 +0.25 156.4 126.8 119.9
19:53 .. 104.4 +0.00 156.1 126.6 116.2

20:04 … 094.2 - 0.50 155.1 125.9 112.4
20:19 … 069.2 -0.73 153.7 124.5 112.9
20:34 … 059.2 -0.81 152.3 123.4 113.5
20:49 … 053.8 -0.87 151.2 122.9 113.6
20:57 … 048.4 -0.90 150.9 122.7 113.5

21:04 … 047.1 -0.80 151.0 122.5 113.5
23:31 … 042.3 -0.89 153.3 122.0 112.2
……………
……………
26:55 … 094.9 -0.90 153.3 121.7 112.3

27:10 … 101.4 -0.67 154.0 121.7 112.3
27:25 … 105.4 -0.57 153.7 121.5 112.3
……………
……………
29:15 … 112.6 -0.47 149.6 119.1 111.2

29:28 … 115.2 -0.10 143.0 118.4 110.7
29:43 CE 115.8 -0.04 147.4 110.1 110.7

16:20 MAX 135.9
18:11 MIN 135.4

Drying pulses 05
CYCLE END 19/11/02
10:17

STERILIZATION: POSITIVE
OPERATOR

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

EXTENDED REPORT
REQUESTED BY THE OPERATOR

---------------------------------------------------------

Report following a

Manual Stop

Model Bravo17
S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0007/0015
Selection 134c POROUS/WRAPPED
Temperature 134 °C
Pressure 2.10 bar
Process time 4 m i n
Stand-by HIGH
Pre-vacuum FRACTIONATED
Drying STANDARD

CYCLE START 19/11/02
11:13

T i m e C bar

---------------------------------------------------------­00:01 CS 077.6 +0.01
01:40 1PV 088.7 -0.80
04:40 1PP 120.6 +1.00
05:40 2PV 062.9 -0.80
07:10 2PP 135.6 +1.00
08:20 3PV 135.5 -0.80
11:20 ET 135.4 +2.15
11:39 SS 135.5 +2.17
12:39 135.5 +2.14
13:39 104.1 +2.15
14:39 047.5 +2.15

STERILIZATION: NEGATIVE

OPERATOR

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

ALARM CODE: E999
DESCRIPTION MANUAL STOP

----------------------------------------------------------

Report following a

Blackout

Model Bravo17
S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0006/0012
Selection 134c CUSTOM
Temperature 134 °C
Pressure 2.10 bar
Process time 07 min
Stand-by HIGH
Pre-vacuum FRACTIONATED
Drying FAST

CYCLE START 19/11/02
15:31

BLACK OUT 19/11/02
15:45

STERILIZATION NEGATIVE
OPERATOR

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

ALARM CODE: E000
DESCRIPTION BLACK-OUT

----------------------------------------------------------

APPENDIX B – PROGRAMS

63.

Report following an alarm

Model Bravo17
S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0007~0015
Selection 134c POROUS/WRAPPED
Temperature 134 °C
Pressure 2.10 Bar
Process time 4 m i n
Stand-by HIGH
Pre-vacuum FRACTIONATED
Drying STANDARD

CYCLE START 19/11/02
11:30

T i m e T1 P T2 T3 T4

------------------------------------------------------------------­00:01 CS 075.1 -0.00 130.9 115.2 093.4
00:11 074.9 -0.28 133.3 114.2 094.0
00:21 074.4 -0.46 146.3 113.2 094.5
00:31 074.3 -0.57 152.6 112.2 095.0
00:35 .. 074.3 -0.59 154.2 111.9 095.2
00:51 .. 078.9 -0.62 152.2 110.4 095.6
01:01 .. 074.9 -0.73 146.6 109.6 095.7
01:27 .. 047.8 -0.78 149.3 107.7 095.7
01:57 .. 047.8 -0.80 155.3 105.8 095.4

02:07 .. 076.5 -0.57 149.9 105.2 095.1
02:17 .. 081.1 -0.49 142.1 104.6 094.6
……………
……………
08:15 … 068.4 -0.76 151.8 104.7 102.3
08:22 … 061.1 -0.80 153.6 104.5 101.7

08:32 ... 097.4 +0.01 154.7 104.0 100.8
08:42 … 104.6 +0.24 148.9 103.7 101.0
……………
……………
15:04 … 135.5 +2.15 143.3 111.7 131.7

15:19 … 135.9 +2.17 148.5 113.5 132.6
15:28 … 135.3 +2.16 153.6 115.9 133.0
……………
……………
19:19 … 135.5 +2.15 157.4 126.5 132.5

19:34 … 134.4 +1.07 157.0 126.8 131.2
19:49 … 108.3 +0.25 156.4 126.8 119.9
19:53 DS 104.4 +0.00 156.1 126.6 116.2

STERILISATION NEGATIVE

ALARM CODE: A112
DESCRIPTION PTC SHORTCIRCUIT

CAUTION !

PLEASE REFER TO USER MANUAL

----------------------------------------------------------

Cycle Report

BOWIE & DICK TEST

Model Bravo17
S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0011/0019
Selection BOWIE&DICK TEST
Temperature 134 °C
Pressure 2.10 bar
Process time 3.5 min

CYCLE START 19/11/02
16:38

T i m e C bar

---------------------------------------------------------­00:01 CS 076.4 +0.00
02:06 1PV 089.3 -0.89
04:35 1PP 120.4 +0.99
05:45 2PV 062.5 -0.78
07:02 2PP 120.2 +0.97
08:15 3PV 061.1 -0.79
11:00 .. 135.6 +2.15
11:14 .. 136.0 +2.17
12:14 135.6 +2.14
13:14 135.6 +2.15
14:14 135.5 +2.14
14:45 .. 135.4 +2.14
15:20 .. 111.5 +0.00
16:34 … 047.8 -0.89
18:21 … 059.5 -0.86
19:21 .. 075.4 -0.50
20:06 CE 078.7 -0.04

12:33 MAX 136.0
14:44 MIN 135.4

Drying pulses 01
CYCLE END 19/11/02
16:38

BOWIE&DICK TEST COMPLETE
Please attach the indicator hereunder

OPERATOR

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

----------------------------------------------------------

Cycle Report

VACUUM TEST

Model Bravo17
S/N 03 BM 0001
Ver. SW Exxxx/BMyyyyyy
Counter 0011/0019
Selection VACUUM TEST

CYCLE START 19/11/02
11:37

T i m e C bar

---------------------------------------------------------­00:00 CS 035.0 +0.00

01:39 E1F 037.4 -0.80
6:39 E2F 038.4 -0.79
16:39 E3F 042.0 -0.79
17:54 CE 045.5 -0.01
CYCLE END 19/11/02

11:41
VACUUM TEST: POSITIVE

OPERATOR

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

----------------------------------------------------------

APPENDIX C – MAINTENANCE

64. .

APPENDIX C - MAINTENANCE

Regular maintenance will guarantee safe, efficient operation of the Bravo over the device's entire life.

For better quality maintenance, supplement ordinary checks with regular periodic
examinations by a qualified technical service department (see Appendix Z).

It is highly recommended users perform a periodic sterilizer validation or ‘check’ of the
thermodynamic parameters of the unit’s processes by comparing them with the reference
values provided with suitably calibrated instruments. In this regard, see “Periodic Sterilizer's
Validation”, below.

The ordinary maintenance described here is easy to complete and involves simple
instruments.

WARNING

ALWAYS USE ORIGINAL REPLACEMENT PARTS.

ROUTINE
MAINTENANCE

Follow this schedule to keep the sterilizer operating at peak efficiency. If units undergo v e r y
intense use, we recommend shortening maintenance intervals. The Bravo unit may remind

you of this schedule on the LCD display.
Refer to the Maintenance Description below for further details.

DAILY

Clean the door gasket
Clean external surfaces

WEEKLY

Clean the sterilization chamber and relative accessories
Disinfect external surfaces

MONTHLY
or 100 cycles

Clean the internal (and external - if installed) distilled water tank
Safety valve maintenance
Clean (or replace) the chamber drain filter

EVERY 3-6 MONTHS
or 400 cycles

Replace bacteriological filter

ANNUAL or every
1000 cycles

Replace the door gasket

EVERY 3 YEARS
or 3000 CYCLES
(by approved
personnel only)

Recommended complete maintenance and calibration of the
sterilizer

General warnings:
– Do not wash the sterilizer with direct jets of water, either under pressure or sprinkled.

Seepage into electrical and electronic components could damage the functioning of the
device or its internal parts;

– Do not use abrasive cloths, metal brushes or metal-cleaning products, whether solids or

liquids, to clean the device or sterilization chamber;

– Do not use chemical products or disinfectants to clean the sterilization chamber. In fact,

these products can irreparably damage the sterilization chamber;

– Do not allow lime residue or other substances to accumulate in the sterilization chamber or

on the door and its gasket. They can damage these parts over time in addition to
compromising the operation of the components installed along the plumbing circuit.

NOTE

THE FORMATION OF WHITE SPOTS ON THE BASE OF THE INTERNAL WALLS OF THE

STERILIZATION CHAMBER IS AN INDICATION THAT YOU ARE USING LOW-QUALITY
DEMINERALIZED WATER.

APPENDIX C – MAINTENANCE

65.

DANGER

BEFORE PERFORMING ORDINARY MAINTENANCE, MAKE SURE THAT
THE POWER SUPPLY CORD IS REMOVED FROM THE MAINS SOCKET.

WHEN IT IS NOT POSSIBLE, TURN OFF THE EXTERNAL BREAKER OF
THE EQUIPMENT POWER SUPPLY LINE.

IF THE EXTERNAL BREAKER IS FAR AWAY OR, AT ANY RATE, NOT
VISIBLE TO THE MAINTAINANCE WORKER, PLACE A WORK IN
PROGRESS SIGN ON THE EXTERNAL BREAKER AFTER TURNING IT OFF.

MAINTENANCE
DESCRIPTION

Clean door gasket and
porthole (door plate)

Clean external surfaces

Clean sterilization
chamber and
accessories

Disinfect external
surfaces

To remove traces of lime, clean the door gasket of the container and the porthole (door plate)
with a clean, cotton cloth soaked in a weak solution of water and vinegar (or similar product).
Dry the surfaces and remove any residue before using the device.

Clean all the external parts using a clean cotton cloth dampened with water and, if needed, a
neutral detergent.
Dry the surfaces and remove any residue before using the device.

Clean the sterilization chamber, support and trays (and internal surfaces in general) with a
clean cotton cloth soaked in water and, if needed, use a small amount of neutral detergent.
Carefully rinse with distilled water, taking care not to leave any type of residue in the chamber
or on accessories.

NOTE

DO NOT USE SHARP OR POINTED INSTRUMENTS TO REMOVE LIME ENCRUSTATION FROM

THE STERILIZATION CHAMB ER. WHEN THERE ARE VISIBLE DEPOSITS, IMMEDIATELY
CHECK THE QUALITY OF THE DISTILLED WATER USED (SEE APPENDIX A,).

For the occasional disinfection of the external surfaces, you can use either denatured alcohol
or detergents with a small percentage of sodium hypochlorite (or equivalent).

APPENDIX C – MAINTENANCE

66. .

Clean internal distilled
water tank

Clean external distilled
water tank

Safety valve
maintenance

Clean/replace the drain
filter

1. Arrange an empty container on the floor near the sterilizer and insert the free end of a
tube.

2. Unscrew the plug (1) from the rear draining point and plug in the other end of the tube.

3. Wait until the internal tank is completely drained and close the draining point with the
plug.

4. Prepare 4 litres / 1.06 US gal of distilled water mixed with 10% of pure alcohol, such as
isopropyl, and fill the supplied standard container

5. Fill the internal tank completely with this solution (see Chapter 5 – Instructions for Use
Filling distilled water for the procedure) and allow the solution to sit for 30 minutes.

WARNING

DO NOT RUN ANY CYCLE DURING THIS PERIOD.

6. Now drain the internal tank and discard the solution. Close the draining point with the
plug.

7. Run one empty (no load) cycle of your choice

1. Disconnect the external tank from the sterilizer and close the tank valve.

2. Fill the tank with a solution of distilled water and alcohol (10%), such as isoproply.

3. Allow the solution to sit for 30 minutes.

4. Drain the tank and discard the solution.

5. Fill the tank with water and drain it, to remove any residual alcohol solution.

6. Reconnect the tank to the sterilizer and refill with distill water.

1. Access the safety valve located on the rear of the machine.

2. Loosen the knurled locking ring with your fingers (or a suitable tool inserted in the two
holes of the ring itself), turning counter-clockwise until it reaches the end and turns
loosely.

3. Retighten the locking ring making sure the threads are properly engaged.

4. Definitively tighten the locking ring all the way down.

WARNING

THE USER SHOULD PERFORM THIS OPERATION MONTHLY TO
GUARANTEE THE CORRECT FUNCTIONING OF THE VALVE OVER TIME.
AT THE END OF THE MAINTENANCE, MAKE SURE THAT THE LOCKING
RING IS COMPLETELY SCREWED ON AND TIGHTENED.

Over time various residues will accumulate inside the filter, obstructing the lower drain tube.
For cleaning (or replace) the filter, open the door of the sterilizer and remove the nut (1) with a

hexagonal wrench no. 14.
Then remove the fitting (2) and the filter (3).
Remove the filter from the support and carefully clean it under running water, using if

necessary a pointed tool to remove possible material of greater dimensions.
If the filter cannot be reused, replace it with a new one.
Reassemble all the parts reversing the order in which you removed the parts. Pay attention on

screwing down the fitting (2) so as to let the draining holes (4) at level of the chamber wall.

APPENDIX C – MAINTENANCE

67.

Replace bacteriological
filter

Replace the door gasket

When it is due to be changed, or when you notice visible clogging of the filter (when the filter
turns gray) unscrew the bacteriological filter from its support and replace it with a new one by
screwing it all the way down on the connector on the front of the machine.

NOTE

A REPLACEMENT BACTERIOLOGICAL FILTER IS SUPPLIED WITH THE DEVICE. TO

REQUEST OTHERS, PLEASE REFER TO APPENDIX Z, TECHNICAL SUPPORT.

Check the inside of the door to ensure it is not hot and then remove the old gasket by hand.
Clean the door gasket seat to ensure it is debris free.

Install the new door gasket by pressing the gasket into its seat, first on top, then bottom, then
both sides. Once seated on 4 sides, continue to press the remaining gasket completely into its
seat

APPENDIX C – MAINTENANCE

68. .

Replacing the printer
paper on units equipped
with internal printers

Printer type 1

1

2

Printer type 2

1

2

3

Periodic sterilizer
calibration and 3000
cycle maintenance

To replace the printer paper:

Printer type1:

1. Open the door (1) of the service compartment to access the printer.

2. Push the tongues (2) to open the printer door and access the paper compartment.

3. Remove the empty roll and place a new roll of thermal paper so that the paper unrolls
from the top.

The roll must have the following dimensions:

- width 57 mm (2.24”) / diameter max 45 mm (1.77”)

4. Unroll about 15 cm (6”) of paper and close the compartment door,

5. Thread the paper in the service compartment door slot and close.

Printer type2:

1. Open the door (1) of the service compartment to access the printer,

2. Push the button (2) on the left to open the printer door (3) and access the paper
compartment,

3. Remove the empty roll and place a new roll of thermal paper so that the paper unrolls
from the top;

The roll must have the following dimensions:

- 57 mm (2.24”) / diameter max 45 mm (1.77”)

4. Unroll about 15 cm (6”) of paper and close the compartment door (the paper will
automatically advance outside the window for several centimeters),

5. Thread the paper in the service compartment door slot and close.

To ensure proper performance of the unit, calibrate the sensors (pressure and temperature),
verify the performance of all major components at least every three years or 3000 cycles

Ensuring the sterilizer is routinely maintained and properly verified over time is the
responsibility of the user.

The 3000 cycle maintenance and calibration procedure requires the use of special equipment
(high-precision reference instruments, calibration tools, dedicated software, etc.) suitably
verified and calibrated in addition to specific experience and training. It is therefore
recommended to contact Technical Service to perform this maintenance

NOTE

THE SCICAN CUSTOMER SUPPORT DEPARTMENT (SEE APPENDIX Z) CAN PROVIDE ANY

INFORMATION RELATIVE TO THE PERIODIC CALIBRATION OF THE STERILIZER.

APPENDIX D – TROUBLESHOOTING

69.

APPENDIX D – TROUBLESHOOTING

Analysis and resolution of problems

If your sterilizer is not working correctly, please consult this list before calling the Technical Service Department:

PROBLEM

POSSIBLE CAUSE

PROPOSED SOLUTION

The sterilizer does not
power-on.

The power cord is not plugged-in.

Plug it in.

There is no voltage at the socket.

Check the cause for the lack of voltage at the socket
and fix it.

The main switch and/or differential
switch are OFF.

Turn the switch ON.

The mains fuses are blown.

Replace with good fuses of equal nominal value.
(See the Summary Table in Appendix A, Technical

Characteristics).

After pressing START,
the sterilization cycle
does not start.

The device is preheating.

Wait for the sterilizer to reach the proper operating
conditions for starting the program.

NOTE: Under normal conditions, the average

preheating time is approx. 10-15 minutes.

The MIN water level
icon is lit.

The distilled water level inside the
tank is below the minimum level.

Fill the distilled water tank until the MAX level indicator
comes on (or, at least, until the MI N level signal turns
off).

The alarm icon is lit.

An alarm was triggered and an
error code and message appear on
the LCD.

Check the alarm code and take the appropriate action.
(See the following paragraphs, Alarms, Alarm Codes

and Troubleshooting).

The safety valve was
triggered.

Locking ring loosened.
Presence of anomalous

overpressure in the chamber.

Check that the knurled locking ring is correctly
tightened on the upper part of the safety valve.

DANGER

LET THE DEVICE COOL, OR
WEAR GLOVES TO AVOID
BEING BURNED WHEN
TOUCHING THE VALVE.

At the end of the
program (CYCLE
COMPLETE), the door
will not open.

There is residual pressure
remaining in the sterilization
chamber at the end of the cycle.

NOTE: the display shows:
N O W LEVELLING

PLEASE WAIT…

Wait several minutes, until the pressure returns to 0.00
bar, and try to open the door again.

Check if the bacteriological filter is clogged and, if
necessary, replace it with a new one.

The procedure for storing the ambient temperature
(SET 0 bar function) was not executed correctly.

Contact the Technical Support Department (see
Appendix Z)

At the end of the cycle, the safety
door lock remains on.

Appendix Z).

There is water leaking
from underneath the
sterilizer.

Drain connectors or tubing (optional
external tank) not correctly
connected to the device.

Check the tightness of the fittings; if necessary,
reassemble, paying more attention to sealing.

Check that the tubes to the drain tank are completely
pushed onto the connectors; make sure that the plastic
ties have been applied.

APPENDIX D – TROUBLESHOOTING

70. .

PROBLEM

POSSIBLE CAUSE

PROPOSED SOLUTION

The water supply tube from the
external tank (optional) is not well
connected.

Check the tightness of the connector; if necessary,
reassemble, paying greater attention to sealing (see
the Chapter 4 - “Installation”).

Check that the tube coming from the external tank is
completely pushed onto the connector; make sure that
the plastic tie has been applied.

Steam leaks from the gasket.

At the end of the cycle, clean the gasket and porthole
of the container under pressure. Check if the gasket is
damaged.
Run another cycle and check the situation. If the
gasket still leaks, replace it with a new one.

There is water around
the drain tank.

Drain tubes (optional drain tank) not
correctly connected to the tank.

Check that the tubes connected to the drain tank are
correctly and completely pushed onto the connectors.

The sterilizer has
problems creating a
vacuum in the chamber
(drying problems,
presence of water in the
sterilization chamber at
the end of the cycle,
etc.).

Drain filter of the sterilization
chamber obstructed.

Clean or replace the drain filter.
(See Appendix C “Maintenance”).

Drain circuit obstructed or drain
tubes choked (optional drain tank).

Check that the drain tubes (and the connectors they
are pushed onto) are not obstructed and run freely
from the device to the tank.

The air intake on the frame and/or
the cover is obstructed or the heat
exchanger is not sufficiently
ventilated.

Remove all possible obstructions from the air intake
and heat exchanger.

Check that the device is not in direct contact with walls
or surfaces (see the Chapter 4 - Installation).

Excessive humidity on
the material and/or
instruments at the end
of the program.

There is too much material inside
the sterilization chamber.

Check the quantity of material sterilized and make sure
that it does not exceed the maximum allowed quantity,
depending on the type of load.

(See the Summary Table in Appendix A, Technical
Characteristics).

Material not correctly positioned.

Position the material, and especially wrapped material,
according to the instructions.

(See the Chapter 7 - Preparing the Material).

Wrong sterilization program
selection

Select the appropriate sterilization program for the type
of material to be treated.

(See the Summary Table in Appendix B, Programs).

Drain filter of the sterilization
chamber obstructed.

Clean or replace the drain filter.
Check for kinks in the exhaust tube, if being used.
(See Appendix C Maintenance).

Traces of oxidation or
spots on instruments

Quality of the instruments is not
adequate.

Check the quality of the instruments with the problem,
checking whether the material they are made of can
tolerate steam sterilization.

Quality of the distilled water not
adequate.

Empty the tank and fill it with high-quality distilled
water.

(See the Water Supply Characteristics in Appendix A,
Technical Characteristics).

Organic or inorganic residues on
the instruments.

Carefully clean the material before subjecting it to the
sterilization cycle.

(See the Chapter 7 - Preparing the Material).

Contact between instruments made
of different metals.

Separate instruments made of different metals.
(See the Chapter 7 - Preparing the Material).

APPENDIX D – TROUBLESHOOTING

71.

PROBLEM

POSSIBLE CAUSE

PROPOSED SOLUTION

Lime residue on the wall of the
sterilization chamber and/or
accessories.

Clean the device and its parts, as required.
(See Appendix C “Ma i n tenance”).

Blackening of the
instruments or damage
to the material.

Wrong sterilization program
selection.

Check the adequacy of the sterilization temperature of
the selected program in relation to the material to be
treated.

(See the Summary Table in Appendix B, Programs).

The printer (optional on
some models) is not
printing the summary
report.

Wrong printer configuration.

Configure the sterilizer for the type of printer used
(Configuration program).

(see the Chapter 6 - Configuration).

Out of paper.

Insert a new roll of paper.
(See Appendix C, Replacing the Paper).

Paper jammed.

Clear the jam.
Check the dimensions of the paper roll.

(See Appendix C, Replacing the Paper).

NOTE

SHOULD ANY OF THESE PROBLEMS PERSIST, CONTACT CUSTOMER SERVICE (SEE APPENDIX Z) PROVIDING THE

MODEL OF THE STERILIZER AND THE SERIAL NUMBER. THIS INFORMATION IS FOUND ON THE SERIAL NUMBER
PLATE ON THE REAR OF THE DEVICE AND ON THE WARRANTY CERTIFICATE.

APPENDIX E – AL AR MS

72. .

APPENDIX E – AL A R M S

ALARMS

Every time an anomalous condition occurs during the operation of the sterilizer, an alarm is
generated and a specific code (consisting of a letter followed by a 3-digit number) is displayed.

Alarm codes are divided into three categories:

• E = ERROR

Operator error or a cause external to the device.
A problem that can generally be fixed by the user.
Code format: Exxx (xxx = identifying number from 000 - 999)

• A = ALARM

First-level fault, not linked to safety.
A problem that normally is fixed by a specialized technician on-site.
Code format: Axxx (xxx = identifying number from 000 - 999)

• H = HAZARD

Second-level fault, linked to safety.
A problem generally fixed by the Technical Support Center.
Code format: Hxxx (xxx = identifying number from 000 - 999)

ALARM
INTERVENTION

Alarm during a c y c l e

NOTE

IN THE CASE OF AN ALARM, DO NOT POWER OFF THE UNIT BEFORE YOU HAVE EXECUTED

A RESET (SEE THE PARAGRAPH, “RESETTING THE SYSTEM”).

An alarm causes the interruption of the cycle with the relative alarm code displayed on the
display, accompanied by a beep and a flashing alarm icon.

NOTE

DURING THE ALARM PROCEDURE, THE DISPLAY ALWAYS SHOWS THE CURRENT

TEMPERATURE AND PRESSURE IN THE STERILIZATION CHAMBER.

This procedure is designed to keep the user from mistaking an anomalous cycle for a correctly
completed cycle and, as a consequence, involuntarily using non-sterile material.

The alarm procedure is differentiated depending on whether it occurs during the execution of
the program or outside, and is structured to guide the user to the necessary RESET of the
sterilizer.

If the alarm intervenes during a program, the display will show the message:

( Alarm Message)

LEVELLING

114.6°C XXXX

0.70 bar 11:30

When an alarm is generated in certain phases of the cycle, an automatic procedure is
activated to clean the internal water circuit. The display will contain the notice:

(Alarm Message)

CIRCUIT CLEANING

100.6°C XXXX

0.70 bar 11:40

Alarm Message

Alarm Code

Alarm Code

APPENDIX E – AL AR MS

73.

Alarm outside
the c y c l e

At the end of what has been described and having reached safe conditions, the machine
activates a special procedure, that asks the user to manually unlock the door:

PRESS ⇑ TO

UNLOCK THE DOOR

101.0°C XXXX

0.01 bar 11:40

NOTE

THE ABOVE INDICATED MESSAGE IS SHOWN ONLY WHEN THE PRESSURE IN THE

CHAMBER IS WITHIN A SAFET LIMIT.

THE RELEASE OF THE LOCKING DEVICE IS NOT POSSIBLE WHEN THE PRESSURE VALUE

IS OUTSIDE THIS LIMIT.

Press the ⇑ key to unlock the door lock mechanism; the following message will appear:

(Alarm Message)

OPEN THE DOOR

100.8°C XXXX

0.01 bar 11:42

Once the door is open, the user is asked to reset the system:

(Alarm Message)

RESET SYSTEM

95.5°C XXXX

0.00 bar 11:43

Perform a RESET (described below) and then turn-off the equipment and check the error or
make the repair.

NOTE

WHEN THE DOOR IS OPENED, THE REPORT (NORMAL OR EXTENDED DEPENDING ON THE

TYPE OF ALARM) WILL BE PRINTED FOR THE INTERRUPTED STERILIZATION PROG RAM
AND THE ALARM THAT INTERVENED. CHECK THE DOCUMENT, INITIAL IT IN THE SPAC E
PROVIDED AND FILE IT IN A SUITABLE PLACE. REFER TO THE PRINT REPORT EXAMPLES
SHOWN IN APPENDIX B, PROGRAMS”.

If the alarm intervenes outside the sterilization or test program, the display will show:

( Alarm Message)

ALARM!

80.5 °C XXXX

0.00 bar

Turn-off the equipment and check the alarm. Or, depending on the type of alarm:

( Alarm Message)

WARNING!

80.5 °C XXXX

0.00 bar

Alarm Message

Alarm Code

Alarm Message

Alarm Code

APPENDIX E – AL AR MS

74. .

which is automatically transformed to the message:

( Alarm Message)

RESET SYSTEM

80.5 °C XXXX

0.00 bar

Perform a RESET (described below) and then turn-off the device and check the alarm.

NOTE

ALARMS THAT INTERVENE OUTSIDE OF A PROGRAM DO NOT PRODUCE A PRINTED

REPORT.

RESETTING THE
SYSTEM

Depending on the alarm, the system must be reset in one of two ways. (see the Alarm Code
List further below in this appendix):

1. Press and hold the PROGRAM SELECTION key for about 3 seconds.

A beep confirms the RESET.

NOTE

NEVER TURN THE DEVICE OFF BEFORE TRYING TO EXECUTE A RESET
AS DESCRIBED ABOVE.

2. Turn-off the device and then power-on using the main switch.

Upon power-up, the sterilizer will perform its normal initial test.

After RESET, and any technical intervention necessary to eliminate the fault, the device will go
to STAND-BY mode, ready to execute a new program.

>3s

APPENDIX E – AL AR MS

75.

ALARM CODES

The list of alarm codes the messages displayed on the LCD and relative RESET mode are as follows:

CODE

ALARM DESCRIPTION

LCD INDICATION

RESET MODE

ERRORS (category E)

E 000

Blackout

BLACK-OUT

Press key

(> 3 seconds)

E 010

Door open

DOOR OPEN

E 020

Exceeded timeout for activating door lock
system (closing)

DOOR UNLOCKED

E 021

Exceeded timeout for activating door lock
system (opening)

DOOR LOCKED

E 030

Water in the fill tank at minimum (MIN) level

WATER MIN

E 031

Water in the drain tank at maximum (MAX) level

EXHAUST MAX

E 041

Filling the tank too frequently
(automatic filling)

FILLING PROBLEM

E 900

Vacuum Test failed
(during the LEAKAGE PHASE)

TEST FAILED

E 901

Vacuum Test failed
(during the WAITING PHASE)

TEST FAILED

E 902

Vacuum Test failed
(vacuum pulse timeout exceeded)

TEST FAILED

E 999

Manual cycle interruption

MANUAL STOP

ALARMS (category A)

A 022

System door lock microswitches failed (OFF­OFF)

LOCKING PROBLEM

Turning-off

device

A 023

System door lock microswitches failed (ON-ON)

LOCKING PROBLEM

A 024

System door lock microswitches failed (ON-OFF)

LOCKING PROBLEM

A 032

Sensor-level problem

LEVEL PROBLEM

A 040

Failure to fill the tank
(automatic filling)

FILLING PROBLEM

A 101

PT1 broken
(sterilization chamber)

PTC BROKEN

A 102

PT2 broken
(steam generator)

PTC BROKEN

A 103

PT3 broken
(heating element)

PTC BROKEN

A 104

PT4 broken
(sterilization chamber wall)

PTC BROKEN

A 111

PT1 short-circuited
(sterilization chamber)

PTC SHORTCIRCUIT

A 112

PT2 short-circuited
(steam generator)

PTC SHORTCIRCUIT

A 113

PT3 short-circuited
(heating element)

PTC SHORTCIRCUIT

A 114

PT4 short-circuited
(sterilization chamber wall)

PTC SHORTCIRCUIT

A200

Pre-heating not performed within the timeout
(heating resistor problem).

HEATING PROBLEM

APPENDIX E – AL AR MS

76. .

CODE

ALARM DESCRIPTION

LCD INDICATION

RESET MODE

A 250

1st vacuum pulse not reached within timeout

PV1 TIMEOUT

Press key

(> 3 seconds)

A 251

1st rise to atmospheric pressure not reached
within timeout

ATM 1 TIMEO U T

A 252

1st pressure pulse not reached within timeout

PP1 TIMEOUT

A 253

2nd vacuum pulse not reached within timeout

PV2 TIMEOUT

A 254

2nd rise to atmospheric pressure not reached
within timeout

ATM 2 TIMEO U T

A 255

2nd pressure pulse not reached within timeout

PP2 TIMEOUT

A 256

3rd vacuum pulse not reached within timeout

PV3 TIMEOUT

A 257

3rd rise to atmospheric pressure not reached
within timeout

ATM 3 TIMEO U T

A 258

3rd pressure pulse not reached within timeout

PPP TIMEOUT

A 259

Phase of PROCESS not started within timeout

PROCESS TIMEOUT

A 260

Chamber depressurization not completed within
timeout

PPD TIME-OUT

HAZARDS (category H)

H 150

MPX pressure sensor broken

MPX BROKEN

Turning-off

device

H 160

MPX pressure sensor short-circuited/not
connected

MPX SHORTCIRCUIT

H 400

Ratio P

conv

/T not balanced (P

conv

>T)

(Phase PROCESS)

P/T PROBLEM

Press key

(> 3 seconds)

H 401

Ratio T/P

conv

not balanced (T>P

conv

)

(Phase PROCESS)

T/P PROBLEM

H 402

Temperature above MAX limit
(Phase PROCESS)

T OVER LIMIT

H 403

Temperature below MIN limit
(Phase PROCESS)

T UNDER LIMIT

H 404

Temperature fluctuating over the limit
(Phase PROCESS)

PT1 FLUCTUATING

H 405

Pressure above MAX limit
(Phase PROCESS)

P OVER LIMIT

H 406

Pressure below MIN limit
(Phase PROCESS)

P UNDER LIMIT

H 410

Wrong maintenance time

(Phase PROCESS)

TIMING PROBLEM

H 990

Excessive pressure
(sterilization chamber, MPX)

OVERPRESSURE

H 991

Overheating
(sterilization chamber, PT1)

OVERHEATING PT1

H 992

Overheating
(steam generator, PT2)

OVERHEATING PT2

H 993

Overheating
(band heating element, PT3)

OVERHEATING PT3

APPENDIX E – AL AR MS

77.

ANALYSIS AND RESOLUTION OF PROBLEMS

Based on the type of alarm, below we provide instructions for identifying the possible causes and restoring correct
operation:

CODE

POSSIBLE CAUSE

PROPOSED SOLUTION

ERRORS (category E)

E 000

Sudden power failure (blackout).

Wait for electricity to return and perform RESET following the
instructions.

Accidentally turning-off the main
switch and/or pulling the plug out of
the socket.

Reconnect the plug and/or power-on the device and perform RESET
following the instructions.

Mains fuses blown.

Replace with good fuses of equal nominal value.
(See the Summary Table in Appendix A, Technical Characteristics”).
Turn-on the device and perform RESET following the instructions.

E 010

Door open (or not properly closed)
at the start of the program
(START).

Perform RESET following the instructions.
Close the door properly and restart the program.

Door position microswitch broken.

Contact the Technical Support Department
(see Appendix Z).

E 020

Limit microswitch (CLOSED
position) of the door lock
mechanism broken.

Perform RESET following the instructions.
Try to start the program a second time.
If the problem persists contact the Technical Support Department

(see Appendix Z).

Door lock system gear motor
broken.

E 021

Limit microswitch (OPEN position)
of the door lock mechanism broken.

Perform RESET following the instructions.

Contact the Technical Support Department
(see Appendix Z).

Door lock system gear motor
broken.

E 030

Water level in the fill tank below
minimum (MIN) level.

Perform RESET following the instructions.
Top-off the water until the MAX level indicator comes on (or at least until

MIN indicator goes off).

MIN water level indicator broken.

Contact the Technical Support Department
(see Appendix Z).

E 031

Water level in the drain tank (or
possible optional external drain
tank) over the MAX level.

Perform RESET following the instructions and empty the tank.
If installed, empty the optional external tank, leaving water up to the level

indicated.

Wire of the optional external tank
level indicator not connected to the
device.

Perform RESET following the instructions.
Connect the plug of the level indicator wire (coming from the optional

external tank) to the female socket located on the back of the device.

MAX water level indicator broken.

Contact the Technical Support Department
(see Appendix Z).

E 041

Connection tube between the
sterilizer and a possible external
filling device is not correctly
installed.

Perform RESET following the instructions.
Check that the water supply tube is correctly and solidly connected to the

relative connectors
Eliminate all possible obstructions along the path of the tube.

External filling container is empty.

Ensure the external filling container is filled with distilled water.

Water filling pump broken.

Contact the Technical Support Department
(see Appendix Z).

Problem in the plumbing circuit.

E 900

Air leaking through the gasket

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

APPENDIX E – AL AR MS

78. .

CODE

POSSIBLE CAUSE

PROPOSED SOLUTION

E 900

Problem in the plumbing circuit.

Contact the Technical Support Department
(see Appendix Z).

E 901

Excessive humidity in the
sterilization chamber.

Perform RESET following the instructions.
Carefully dry the inside of the sterilization chamber and start the program

again.

Air leaking through the gasket

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

Problem in the plumbing circuit.

Contact the Technical Support Department
(see Appendix Z).

E 902

Excessive humidity in the
sterilization chamber.

Perform RESET following the instructions.
Carefully dry the inside of the sterilization chamber and start the program

again.

Air leaking through the gasket

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

Vacuum pump broken.

Contact the Technical Support Department
(see Appendix Z).

Problem in the plumbing circuit.

E 999

Manual interruption of
sterilization or test program.

(Also see the Chapter 9 -
“Running the Program”)

Perform RESET following the instructions.
Check that the load has been correctly sterilized, by reading the LCD

display, before using the material.

ALARMS (category A)

A 022

Limit microswitch(es) on the door
lock mechanism broken.

Contact the Technical Support Department
(see Appendix Z).

A 023

Limit microswitch(es) on the door
lock mechanism broken.

A 024

Limit microswitch(es) on the door
lock mechanism broken.

A 032

Connector of the water level
indicators not connected.

Level indicator(s) broken.

A 040

Lack of water in the external tank or
Bravo Pure turned off (automatic
filling).

Perform RESET following the instructions.
Fill the tank with a sufficient quantity of water, remembering to

periodically check the level, or turn on the Bravo Pure.

Connection tube between the
sterilizer and a possible external
filling device not correctly installed.

Perform RESET following the instructions.
Check that the water supply tube is correctly and solidly connected to the

relative connectors.
Eliminate all possible obstructions along the path of the tube.

Water filling pump broken.

Contact the Technical Support Department
(see Appendix Z).

A 101

Chamber temperature sensor (PT1)
broken.

Contact the Technical Support Department
(see Appendix Z).

A 102

Steam generator temperature
sensor (PT2) broken.

A 103

Heating element temperature
sensor (PT3) broken.

A 104

Chamber wall temperature sensor
(PT4) broken.

APPENDIX E – AL AR MS

79.

CODE

POSSIBLE CAUSE

PROPOSED SOLUTION

A 111

Incorrect connection of the

temperature sensor (sterilization
chamber) to the connector.

Contact the Technical Support Department
(see Appendix Z).

Temperature sensor short circuit
(sterilization chamber).

A 112

Incorrect connection of the

temperature sensor (steam
generator) to the connector.

Temperature sensor short circuit
(steam generator).

A 113

Incorrect connection of the

temperature sensor (heating
element) to the connector.

Temperature sensor short circuit
(heating element).

A 114

Incorrect connection of the

temperature sensor (chamber wall)
to the connector.

Temperature sensor short circuit
(chamber wall).

A 200

Intervention of the steam generator
safety thermostat.

Manually rearm the thermostat(s) located on the back of the device (see
the Chapter 3 - Product Overview)

Unscrew the black plastic protection cap, press the white button until
you hear a click and replace the cap.

Turn-off (RESET) and then turn-on the device.
If the problem persists contact the Technical Support Department

(see Appendix Z).

Intervention of the heating element
safety thermostat.

Heating or steam generator heating
element malfunction.

A 250

Presence of water or condensate in
the sterilization chamber.

Perform RESET following the instructions.
Carefully dry the inside of the sterilization chamber and start the program

again.
Do not put material impregnated with water, or liquids in general, in the

chamber.

Drain filter of the sterilization
chamber obstructed.

Clean or replace the drain filter.
(See Appendix C “Maintenance”).

Air leaking through the gasket.

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

Vacuum pump broken.

Contact the Technical Support Department (see Appendix Z).

Problem in the plumbing circuit.

A 251

Water injection pump malfunction.

Contact the Technical Support Department (see Appendix Z).

Problem in the plumbing circuit.

Intervention of the steam generator
safety thermostat.

Manually rearm the thermostat(s) located on the back of the device (see
the Chapter 3 - Product Overview).

Unscrew the black plastic protection cap, press the white button until
you hear a click and replace the cap.

Turn-off (RESET) and then turn-on the device.
If the problem persists, contact the Technical Support Department (see

Appendix Z)

Heating element safety thermostat
intervened.

Contact the Technical Support Department (see Appendix Z).
Heating or steam generator heating

element malfunction.

APPENDIX E – AL AR MS

80. .

CODE

POSSIBLE CAUSE

PROPOSED SOLUTION

A 252

Steam leaking through the gasket.

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

Excessive load.

Perform RESET following the instructions.
Check the quantity of material in the sterilization chamber and make sure

it does not exceed the maximum quantity allowed.
(See the Summary Table in Appendix A, Technical Characteristics).

Problem in the plumbing circuit.

Contact the Technical Support Department (see Appendix Z).

Intervention of the steam generator
safety thermostat.

Manually rearm the thermostat(s) located on the back of the device (see
the Chapter 3 -Product Introduction).

Unscrew the black plastic protection cap, press the white button until
you hear a click and replace the cap.

Turn-off (RESET) and then turn-on the device.
If the problem persists, Contact the Technical Support Department (see

Appendix Z).

Heating element safety thermostat
intervened.

Contact the Technical Support Department
(see Appendix Z).

Heating or steam generator heating
element malfunction.

A 253

Presence of water or condensate in
the sterilization chamber.

Perform RESET following the instructions.
Carefully dry the inside of the sterilization chamber and start the program

again.
Do not put material impregnated with water, or liquids in general, in the

chamber.

Air leaking through the gasket.

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

Vacuum pump broken.

Contact the Technical Support Department
(see Appendix Z).

Problem in the plumbing circuit.

A 254

Water injection pump malfunction.

Contact the Technical Support Department
(see Appendix Z).

Problem in the plumbing circuit.

Intervention of the steam generator
safety thermostat.

Manually rearm the thermostat(s) located on the back of the device (see
the Chapter 3 - Product Overview).

Unscrew the black plastic protection cap, press the white button until
you hear a click and replace the cap.

Turn-off (RESET) and then turn-on the device.
If the problem persists, contact the Technical Support Department (see

Appendix Z).

Heating element safety thermostat
intervened.

Contact the Technical Support Department
(see Appendix Z).

Heating or steam generator heating
element malfunction.

A 255

Steam leaking through the gasket.

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

APPENDIX E – AL AR MS

81.

CODE

POSSIBLE CAUSE

PROPOSED SOLUTION

A 255

Excessive load.

Perform RESET following the instructions.
Check the quantity of material in the sterilization chamber and make sure

it does not exceed the maximum quantity allowed.
(See the Summary Table in Appendix A, Technical Characteristics).

Problem in the plumbing circuit.

Contact the Technical Support Department
(see Appendix Z).

A 255

(continue)

Intervention of the steam generator
safety thermostat.

Manually rearm the thermostat(s) located on the back of the device (see
the Chapter 3 - Product Overview).

Unscrew the black plastic protection cap, press the white button until
you hear a click and replace the cap.

Turn-off (RESET) and then turn-on the device.
If the problem persists, Contact the Technical Support Department (see

Appendix Z).

Heating element safety thermostat
intervened.

Contact the Technical Support Department
(see Appendix Z).

Heating or steam generator heating
element malfunction.

A 256

Presence of water or condensate in
the sterilization chamber.

Perform RESET following the instructions.
Carefully dry the inside of the sterilization chamber and start the program

again.
Do not put material impregnated with water, or liquids in general, in the

chamber.

Air leaking through the gasket.

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water.
Start the program again. If the gasket still leaks, replace the gasket.

Vacuum pump broken.

Contact the Technical Support Department
(see Appendix Z).

Problem in the plumbing circuit.

A 257

Water injection pump malfunction.

Contact the Technical Support Department
(see Appendix Z).

Problem in the plumbing circuit.

Intervention of the steam generator
safety thermostat.

Manually rearm the thermostat(s) located on the back of the device (see
the Chapter 3 - Product Overview).

Unscrew the black plastic protection cap, press the white button until
you hear a click and replace the cap.

Turn-off (RESET) and then turn-on the device.
If the problem persists, Contact the Technical Support Department (see

Appendix Z).

Heating element safety thermostat
intervened.

Contact the Technical Support Department
(see Appendix Z).

Heating or steam generator heating
element malfunction.

A 258

Steam leaking through the gasket.

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water, and start the program again. If the gasket still leaks, replace the
gasket.

Excessive load.

Perform RESET following the instructions.
Check the quantity of the material in the sterilization chamber and make

sure that it does not exceed the maximum allowed quantity, depending
on the type of load.

(See the Summary Table in Appendix A, Technical Characteristics).

Problem in the plumbing circuit.

Contact the Technical Support Department (see Appendix Z).

APPENDIX E – AL AR MS

82. .

CODE

POSSIBLE CAUSE

PROPOSED SOLUTION

A258

Intervention of the steam generator
safety thermostat.

Manually rearm the thermostat(s) located on the back of the device (see
the Chapter 3 - Product Overview).

Unscrew the black plastic protection cap, press the white button until
you hear a click and replace the cap.
Turn-off (RESET) and then turn-on the device.

If the problem persists, Contact the Technical Support Department (see
Appendix Z).

Heating element safety thermostat
intervened.

Contact the Technical Support Department
(see Appendix Z).

Heating or steam generator heating
element malfunction.

A 259

Excessive load.

Perform RESET following the instructions.
Check the quantity of the material in the sterilization chamber and make

sure that it does not exceed the maximum allowed quantity, depending
on the type of load.

(See the Summary Table in Appendix A, Technical Characteristics).

Steam leaking through the gasket.

Perform RESET following the instructions.
Carefully clean the gasket with a clean cotton cloth dampened with

water, and start the program again. If the gasket still leaks, replace the
gasket.

Problem in the plumbing circuit.

Contact the Technical Support Department
(see Appendix Z).

A 260

Problem in the plumbing circuit.

HAZARDS (category H)

H 150

Pressure sensor (MPX) broken.

Contact the Technical Support Department
(see Appendix Z).

H 160

Incorrect connection of the

pressure sensor (MPX) to the
connector.

Pressure sensor (MPX) short
circuit.

H 400

Problem in the plumbing circuit.

H 401

Problem in the plumbing circuit.

H 402

Steam generator malfunction.

Problem in the plumbing circuit.

H 403

Steam generator malfunction.

Problem in the plumbing circuit.

H 404

Problem in the plumbing circuit.

Steam generator malfunction.

H 405

Problem in the plumbing circuit.

Steam generator malfunction.

H 406

Problem in the plumbing circuit.

Steam generator malfunction.

H 410

Timer problem

H 990

General operating problem.

H 991

General operating problem.

H 992

General operating problem.

H 993

General operating problem.

APPENDIX F – DIAG RAMS

83.

APPENDIX F – DIAGRAMS

ELECTRICAL DIAGRAM

APPENDIX F – DIAG RAMS

84. .

PLUMBING DIAGRAM

APPENDIX G – NOTES

85.

APPENDIX G - NOTES

APPENDIX H – SPARE PARTS & ACCESSORIES

86. .

APPENDIX H – SPARE PARTS & ACCESSORIES

Description

Part Number

Door Gasket, Bravo

48000050000

Biological Filter, Bravo

47200010000

Chamber Drain Filter, Bravo

47200030000

Thermal Paper

STXX0250000

Data Logger (G), Bravo

01-111729

Data Logger (T), Bravo

01-111730

Water In-Take Pull Kit, Bravo

01-111774S

Direct-to-Drain Kit, Bravo

01-111775S

Rack Chamber, Bravo 17(V)

C1BP583000Y

Rack Chamber, Bravo 21V

C1BG534000Y

Tray 17/17V, Bravo

C1BP583000Y

Tray 21V, Bravo

C1BG534000Y

Pouch Rack, Bravo

C1BP553000Y

Tray Extractor, Bravo

STXX0080000

Drain Pipe, Bravo

110000003W0

Water Filling Jug

A0XP0010000

Mounting Feet, Bravo

25600000400

APPENDIX I – TECHNICAL SUPPORT

87.

APPENDIX I – TECHNICAL SUPPORT

For all service and repair inquiries:

Canada 1-800-870-7777
United States: 1-800-572-1211
International: [phone]
Email: [e-mail] (Canada)

[e-mail] (USA)
[e-mail] (International)

88. .

APPENDIX J – LIMITED WARRANTY

APPENDIX J – LIMITED WARRANTY

For a period of two years or 2500 cycles, which ever appears first, SciCan guarantees that the Bravo Autoclave,
when manufactured by SciCan in new and unused condition, will not fail during normal service due to defects in
material and workmanship that are not due to apparent abuse, misuse, or accident.

The two year warranty will cover the performance of all components of the unit except consumables such as

the

d

oor seal, microbiological filter, water filter, wire racks and trays, provided that the product is being used and

maintained according to the description in the operator’s manual.
In the event of failure due to such defects during this period of time, the exclusive remedies shall be repaired or

replaced, at SciCan’s option and without charge, of any defective non-consumable part(s) (except gasket),
provided SciCan is notified in writing within thirty (30) days of the date of such a failure and further provided that
the defective part(s) are returned to SciCan, prepaid.

This warranty shall be considered to be validated if the product is accompanied by the original purchase invoice
from the authorized SciCan dealer, and such invoice identifies the item by serial number and clearly states the
date of purchase. No other validation is acceptable. After two years or 2500 cycles, all SciCan’s warranties and
other duties with respect to the quality of the product shall be conclusively presumed to have been satisfied. All
liability therefore shall be terminated, and no action or breach of any such warranty or duty may thereafter be
commenced against SciCan.

Any express warranty not provided hereon and any implied warranty or representation as to performance, and
any remedy for breach of contract which, but for this provision, might arise by implication, operation of law,
custom or trade or course of dealing, including any implied warranty of merchantability or of fitness for particular
purpose with respect to all and any products manufactured by SciCan is excluded and disclaimed by SciCan.

89.