Your facility has selected the leading-edge
medical technology made by MAQUET.
We sincerely appreciate the trust you have
placed in us.
MAQUET is a member of the GETINGE group
which is consistently directing its attention to
pioneering medico-technical solutions.
1.2How to use these operating instructions
1.2.1General
These operating instructions are provided to
familiarise you with the features of this
MAQUET product. They are subdivided into
several chapters.
MAQUET is one of the world’s leading suppliers
for emergency rooms, operating rooms and
intensive care units. MAQUET has been
standing for innovation and advance in medical
technology ever since it was founded in 1838.
Solutions relevant to the needs of practice and
customer-oriented services optimise working
cycles and boost economy in hospitals – all to
the benefit of the patient.
Please note:
• Please read these operating instructions
carefully and completely before using the
product for the first time.
• Always proceed in accordance with the
information contained herein.
• Store these operating instructions in a
location near the product.
1.2.2Abbreviations
EMCElectromagnetic compatibility
ENEuropean standard
EUEuropean Economic Community
IRInfrared
INTIntermittent
IPSInternal Power Source
LEDLight Emitting Diode
OR tableOperating table
PURPolyurethane integral foam
SELVSafety Extra Low Voltage
SFCSoft Foam Core (special foam core)
1433.01XX
GA 1433.01 EN 08
1
Introduction
1
How to use these operating instructions
1.2.3Symbols
1.2.3.1Order number
An "X" in the order number (e.g. 1122.33X4) is
a placeholder for a number of variants.
1.2.3.2Cross-references
References to other pages in these operating
instructions are identified with a double arrow
symbol "
1.2.3.3Actions and responses
The "
the user while the "
reaction that this will induce in the system.
".
" symbol identifies an action taken by
" symbol identifies the
Example:
Turn on the light switch.
Lamp lights up.
1.2.3.4Buttons and menus
Buttons and menus are enclosed in square
brackets.
Example:
Press the [DOWN] button in the [Operation]
menu.
1433.01XX
2
GA 1433.01 EN 08
1.2.4Definitions
1.2.4.1Design of safety notes
PictogramDescriptorText
D ANGER!
How to use these operating instructions
Indicates a direct and immediate risk
to persons, which may be fatal or
result in most serious injury.
Introduction
1
The text for the safety
note describes the type
of risk and how to avert
it.
W ARNING!
C AUTION!
Fig. 1: Design of safety notes
1.2.4.2Design for other notes
Notes not referring to personal injury or
property damage are used as follows:
PictogramDescriptorReference to
N OTE
E NVIRONMENT
Indicates a potential risk to persons
or property which may result in health
hazard or grave property damage.
Indicates a potential risk to property
which may result in property damage.
Supplementary assistance or further useful information.
Proper disposal.
Fig. 2: Design for other notes
1433.01XX
GA 1433.01 EN 08
3
Introduction
1
How to use these operating instructions
1.2.4.3Definition for 3-dimensional coordinate system
The "permissible overall load" results from adding up patient weight, side rail accessory weight
and positioning aids. The "permissible overall
load" is the load which may be put on the table
top.
1.2.4.6Definition of protrusion
Protrusion is the gap between the mounting
point(s) of a table top to the relevant outer edge
of the table top components (e.g. head rest, leg
plates) applied to the front.
1.2.4.7Definition of area prone to explosion, Zone AP-M
The medical environment is designated as
"Zone AP-M" (1).
Restrictions might result from the components
table top and transporter for which other overall
loads may be valid, or from special patient positions.
The maximum protrusion of a table top may not
be exceeded.
Fig. 5: Area prone to explosion, Zone AP-M
1.2.4.8Definition Positioning- / Transporting
When moving, a distinction is made between
moving the mobile operating table with a patient
and without a patient.
Positioning
Positioning refers to the process of moving the
mobile operating table with a patient within the
operating room.
Transporting
Transporting refers to the process of moving
the mobile operating table without a patient in
the operating room.
1433.01XX
GA 1433.01 EN 08
5
Introduction
12
1
How to use these operating instructions
1.2.4.9Definition of travelling forwards / backwards
Fig. 6: Travelling forwards / backwards
The following definition applies to motor-powered motion:
• forwards (1)
• backwards (2)
1433.01XX
6
GA 1433.01 EN 08
1.2.4.10Definition of patient orientation
1
1
W ARNING!
Risk of injury!
Incorrectly adjusted patient orientation may cause adjustment of the
operating table in a direction that was not intended.
Check the correct patient orientation prior to making any adjustments.
The patient orientation is indicated in the status bar on the display on the hand
control.
The patient orientation depends on the position
of the patient on the table top with regard to the
operating table base (1).
NORMAL patient orientation
Introduction
How to use these operating instructions
The upper part of the patient's body is located
above the longer section of the operating table
base (1).
1
Fig. 7: NORMAL patient orientation
REVERSE patient orientation
Fig. 8: REVERSE patient orientation
The legs are located above the longer section
of the operating table base (1).
1433.01XX
GA 1433.01 EN 08
7
Introduction
1
How to use these operating instructions
1.2.5Symbols used
Symbols are attached to products, type plates and packaging.
SymbolsIdentification
Labelling for Class I products, developed and marketed in compliance with
Medical Device Directive 93/42/EU.
Labelling in compliance with the ISO 15223-1 standard.
Symbol for "Product number"
Labelling in compliance with the ISO 15223 -1 standard.
Symbol for "Serial number".
Designation in compliance with the ISO 15223-1 standard.
Symbol for "Name and address of the manufacturer as well as date of
manufacture".
Labelling in compliance with the IEC 60601-1 standard.
Symbol for "Follow Operating Instructions".
Labelling in compliance with the IEC 60601-1 standard.
Symbol for "Observe the accompanying documents".
Symbol for "Observe operating instructions".
Labelling for devices incorporating a Type B applied part as defined in the
IEC 60601-1 standard.
Degree of protection against electric shock.
Labelling in compliance with the IEC 60601-1 standard.
Symbol for "Class II".
Labelling as per 2002/96/EU Directive
(Directive on Waste Electrical and Electronic Equipment).
Symbol for "Do not dispose of at the municipal collection points for used
electrical equipment".
1433.01XX
8
GA 1433.01 EN 08
Labelling as per IEC 60529 standard.
Symbol for "splash protection".
Fig. 9: Symbols (Part 1 of 2)
SymbolsIdentification
Labelling in compliance with the IEC 60601-1 standard.
Symbol for "Potential equalisation".
Labelling of Category AP equipment as per the IEC 60601-1 standard.
Explosion protection by avoiding sources of ignition when using flammable
blends of anaesthetics which are mixed with air, oxygen or nitrous oxide.
Labelling in compliance with the BGV A 8 Accident Prevention Regulations
(previously VBG 125).
Symbol for "Risk of pinching and crushing".
Packaging label.
Symbol for "Keep dry".
Introduction
How to use these operating instructions
1
Packaging label.
Symbol for "Fragile! Handle with care".
Packaging label.
Symbol for "Top".
Labelling in compliance with the ISO 15223 -1 standard.
Symbol for "Temperature range".
Labelling in compliance with the ISO 15223-1.
Symbol for "Relative humidity".
Labelling in compliance with the ISO 15223-1.
Symbol for "Air pressure".
Fig. 9: Symbols (Part 2 of 2)
1433.01XX
GA 1433.01 EN 08
9
Introduction
1
Disposal
1.3Disposal
1.3.1General
Used products or parts thereof may be contaminated. To prevent potential infection, please
clean and disinfect the product prior to return/disposal.
1.3.2Packing
The packing is made of materials compatible
with the environment. MAQUET will dispose of
the packing materials upon request.
1.3.3Padding
Padding can be disposed of as normal household waste.
1.3.4Rechargeable batteries/ Batteries
Rechargeable batteries/batteries can be turned
in to your local disposal system.
1.3.5MAQUET products
MAQUET will take back used products or those
which are no longer in service.
1.3.6Used electrical equipment
1.3.6.1Within the European Economic Community
This product is governed by the 2002/96/EU Directive (Directive on Waste Electrical and Electronic Equipment).
This product has not been registered for use in
private households; disposal using municipal
1.3.6.2Outside the European Economic Community
When disposing of this product, ensure compliance with the applicable national regulations on
the handling and disposal of used equipment.
Please contact your MAQUET representative
for more detailed information.
collection points for used electrical equipment
is not permitted.
Please contact your MAQUET representative
for more detailed information on correct and legal disposal.
10
1433.01XX
GA 1433.01 EN 08
1.4Overview
7
6
8
1
12
10
3
11
15
9
14
13
19
18
17
15
16
14
5
1a
1b
2
4
Introduction
Overview
1
Fig. 10: Overview of OR table (1433.01XX)
1 Extension device (1433.62A1), optional:
Screw tension device (1a)
Gas strut assisted height adjustment (1b)
2 Extension shoe (1003.67C0), optional
3 Traction bar (1433.61AC), optional
4 Extension plate (1433.66AC), optional
5 Extension plate (1433.66BC), optional
6 Extension plate (1131.31BC), optional
7 NORMAL mounting point
8 Basic table top
9 Release button for traction bar
10 Connection for equipotential bonding
11 Connection for mains cable
12 Service mounting point
13 Override control panel
14 Connections for corded hand control / foot
switch
15 Infrared receiver
16 REVERSE mounting point
17 IR remote control (1433.91A0), optional
18 Corded hand control (1433.90A0), optional
19 Foot switch (1009.81GX), optional
1433.01XX
GA 1433.01 EN 08
11
Introduction
1
Basic requirements
1.5Basic requirements
1.5.1Use in accordance with the intended purpose
This product is an active Class I medical device
according to the Medical Device Directive
93/42/EU, which will have to be entered in the
medical device log.
In accordance with the above-mentioned
Directive, the only persons who may operate
this product are those who have been instructed, by authorised personnel, in the use of the
product.
This product is to be used exclusively in human
medicine.
Patients may be placed on the device and
brought into position only under the supervision
of medical personnel.
1.5.2Applicable standards
The product satisfies the basic requirements
set forth in Annex I to the 93/42/EU Directive
drafted by the Medical Products Council
(Medical Device Directive) as well as the
applicable national codes and the Medical
Rooms used for medical purposes and in which
the product is used shall comply with
VDE Regulation 0100 Part 710 and/or the corresponding local codes.
Accessories
Accessories or combinations of accessories
may be utilised only when and as indicated in
these operating instructions.
Use other accessories, combinations and parts
subject to wear only if these are intended
expressly for the application and will not
adversely affect performance features or safety
requirements.
Products Act in Germany. This is certified by
compliance with harmonised standards such as
IEC 60601-1 and related standards and the
respective special sections.
12
1433.01XX
GA 1433.01 EN 08
1.5.3Intended purposes
1.5.3.1Mobile operating table YUNO
Introduction
Basic requirements
1
The YUNO mobile operating table (1433.01XX)
is designed for the support and positioning the
patient for surgical treatment immediately before, during and after surgical interventions as
well as for examination and treatment.
The table top is radiolucent and enables intraoperative use of X-ray equipment. The design
of the table top makes the OR table suitable for
all surgical disciplines.
The product may only be operated by medically
trained staff within the OR environment. Any
use other than described above is deemed not
to be in accordance with the intended purpose.
The OR table can be used for an overall load of
up to 155 kg without restrictions on positions
and adjustment functions. The OR table can be
1.5.3.2Variants
The product is available in the following versions:
• 1433.01B0
with SFC padding, side rails in EUROPE format (10 x 25 mm) and autodrive
• 1433.01F0
with SFC padding, side rails in USA format
(9.54 x 28.6 mm) and autodrive
used with restrictions with an overall table top
load between 155 kg and 454 kg.
In conjunction with the extension device
(1433.62A1), the OR table can be used without
restrictions up to 250 kg.
The OR table (1433.01XX) may not be used
under the following conditions:
• if the overall load exceeds 454 kg,
• if the overall load exceeds 155 kg, without
taking restrictions into account,
• to transport the patient within the hospital,
• with accessories which are not approved by
MAQUET,
• in rooms where MR tomographs are employed.
1.5.3.3Product features
All materials used by MAQUET (e.g. materials
used for SFC and PUR padding, gel pads,
belts, transport belts, etc.) are latex-free.
1433.01XX
GA 1433.01 EN 08
13
Introduction
1
Basic requirements
1.5.3.4Hand controls
The hand controls are used to adjust the OR table.
1.5.3.5Side rails
Side rails are used to mount approved
accessories, in accordance with the
manufacturer's instructions.
The following distinctions are made:
• Corded hand control (1433.90A0)
• IR remote control (1433.91A0)
• Foot switch (1009.81G0/G1/G2)
• Override control panel on the column (integrated into the column)
14
1433.01XX
GA 1433.01 EN 08
2Basic safety instructions
2.1Personal safety notes
D ANGER!
Potentially fatal!
Hazard resulting from improper handling.
Be absolutely sure to follow the operating instructions for the operating table.
D ANGER!
Potentially fatal!
Risk caused by incorrect handling.
Please always observe the technical description for the mobile operating table.
W ARNING!
Risk of injury!
Patient may be endangered as a result of incorrect use.
Follow the operating instructions for all accessories.
Basic safety instructions
Personal safety notes
2
D ANGER!
Potentially fatal!
Danger due to unauthorised modifications.
The product may not be modified.
D ANGER!
Potentially fatal!
Vital functions can be impaired through incorrect positioning.
Position the patient correctly and maintain continuous observation.
W ARNING!
Risk of injury!
Improper positioning can be detrimental to patient health (causing bedsores, for
instance).
Always position the patient correctly and maintain continuous observation.
W ARNING!
Injury hazard!
MAQUET products may be used only when fully functional.
Check to ensure that this MAQUET product is fully functional and in good working
order prior to use.
W ARNING!
Risk of injury!
MAQUET products may be used only when properly lubricated.
Lubricate MAQUET products at regular intervals.
GA 1433.01 EN 08
1433.01XX
15
Basic safety instructions
2
Personal safety notes
D ANGER!
Risk of explosion!
The operating table may not be used in hazardous locations (AP-M) during mains
operation.
An explosion could occur when using disinfectants or cleaning agents containing
alcohol, or flammable anaesthetics which are blended with air, oxygen or nitrous
oxide.
When operating on the mains supply, never use disinfectants or cleaning agents
containing alcohol, or flammable anaesthetics which are blended with air, oxygen
or nitrous oxide!
W ARNING!
Risk of injury!
Park the mobile operating table on level ground and secure with the [LOCK] func-
tion before each application and after each movement.
W ARNING!
Risk of injury!
Park the mobile operating table on level ground and secure with the [LOCK] func-
tion before each application and after each movement.
W ARNING!
Risk of injury due to material breakage or tipping of the OR table!
The accessories attached to the OR table may not exceed the maximum protru-
sion (protrusion = maximum distance to leg plate/back plate mounting point of the
OR table, see section on patient positioning).
The accessory can be deployed without restriction within the permitted overhang
of the OR table and up to a proportionate patient weight of 135 kg.
If the overall load is between 155 kg to maximum 454 kg, the protrusion of the OR
table and all accessories used must be authorised for such use respectively.
Please observe these specifications for positioning the patient.
W ARNING!
Risk of injury due to the OR table tipping!
With an overall load of in excess of 250 kg, do not extend the swivel castors of the
mobile operating table.
Function [UNLOCK] is not permitted.
16
W ARNING!
Injury hazard resulting from the operating table tipping!
Observe the prescribed orientation for the patient.
Do not lay the patient's upper part of the body on the leg plates.
1433.01XX
GA 1433.01 EN 08
Basic safety instructions
Personal safety notes
W ARNING!
Risk of injury due to the operating table tipping!
If the patient is transferred to the operating table over the head end of the
operating table, the operating table may tip.
The patient may be transferred only from the side of the operating table.
W ARNING!
Risk of injury due to the operating table tipping!
If the operating table is not locked during patient transfer, the operating table may
tip.
The operating table must be locked on the floor before transferring the patient.
W ARNING!
Risk of injury!
If the patient is not secured during positioning of the OR table, when adjusting the
table top or when positioning the patient (particularly when the inclination and tilt
features are used), the patient could slip, uncontrolled, off the table top.
Always secure the patient and maintain continuous observation.
2
W ARNING!
Injury hazard!
When adjusting or moving the operating table or table top, the staff, the patient
and the accessories are exposed to pinching and shearing hazards, particularly
in the area around the joints at the head, back and leg plates.
Always ensure that no one can be subjected to pinching or shearing action or
injured in any other way and the accessories do not collide with any nearby
objects.
W ARNING!
Risk of injury!
Whenever the product is mounted and adjusted, there is a danger of pinching and
shearing to the staff, patient and accessories.
Always ensure that no one can be subjected to pinching or shearing action or
injured in any other way and that the accessories do not collide with any nearby
objects.
W ARNING!
Risk of injury!
If the individual adjustment function for a divided leg plate is activated at the joint
mounting point, although a single-piece accessory is attached to the mounting
point, the accessory may be damaged during individual adjustment in the event
of a malfunction.
Before adjusting single-piece accessories ensure that the individual adjustment
function is deactivated using the selector switch [leg side] (status LEDs for the left
and right leg side are on).
1433.01XX
GA 1433.01 EN 08
17
Basic safety instructions
2
Personal safety notes
W ARNING!
Risk of injury!
When setting down the OR table, feet or objects lying on the floor may get pinched
or crushed.
Before setting the OR table down, make sure that there are neither feet nor any
objects underneath the column.
W ARNING!
Injury hazard!
Electrical devices (e. g. cellphones, radios, magnetic resonance tomographs) can
interfere with the functioning of the product when used near the product.
Electrical devices which can interfere with the functioning of the product may not
be used near the product.
Please observe the information concerning electromagnetic compatibility (EMC)
(radiation and resistance to interference) contained in the Technical Description.
Adhere to those specifications when using electrical devices and respond proper-
ly in the event of effects on the device or the product.
W ARNING!
Risk of burning!
Using high-frequency devices, defibrillators and defibrillator monitors exposes the
patient to burn hazard due to contact with metal components in the device or
accessories and/or if resting on wet drapes or electrically conductive padding.
Avoid any contact between the patient and metallic components; never use moist
of wet surgical drapes.
Be absolutely sure to comply with the manufacturers operating instructions!
W ARNING!
Risk of injury!
Magnetic fields of a magnitude of more than 0.5 mT may impair the function of the
product.
Never use the product within the 0.5 mT field.
W ARNING!
Risk of infection!
If the operating table is used in areas with varying hygienic requirements, there is
a risk of infection.
Treat the operating table in accordance with the hygiene guideline and the
instructions given in the chapter "Cleaning and disinfection".
18
1433.01XX
GA 1433.01 EN 08
2.2Safety notes for the OR table
W ARNING!
Risk of injury!
If locking elements (offset levers, handle screws, locking mechanisms etc.) are
opened, the clamps are released and the product can be moved.
Before opening the locking elements, hold the individual parts securely. Make
sure that all locking elements are closed after each adjustment procedure.
C AUTION!
Property damage!
Eliminate all potential hindrances and obstacles before moving the operating
table and avoid collisions.
C AUTION!
Property damage!
When tilting or sloping the table top or when articulating the leg plate ensure that
the table top does not collide with the column or the operating table base.
Basic safety instructions
Safety notes for the OR table
2
C AUTION!
Property damage!
Any objects left on the operating table base will damage the cladding as it moves.
Do not put any objects on the operating table base.
1433.01XX
GA 1433.01 EN 08
19
Basic safety instructions
2
Safety notes regarding the use of accessories
2.3Safety notes regarding the use of accessories
W ARNING!
Risk of injury due to material failure!
The side rail accessory weight may not exceed 25 kg.
The maximum permissible overall load is reduced in accordance with the weight
of the accessories attached. Never use accessories weighing more than this max-
imum.
W ARNING!
Risk of injury!
Patient may be endangered as a result of incorrect use.
Follow the operating instructions for all accessories.
W ARNING!
Risk of injury!
Accessories that are not approved by MAQUET for this product as well as acces-
sories from other manufacturers may cause injuries.
Only use MAQUET accessories that have been approved for the product.
Accessories made by other manufacturers may only be used after obtaining writ-
ten permission from MAQUET.
W ARNING!
Risk of injury!
When adjusting and moving the OR table, the table top or the accessories colli-
sions may occur with the patient, between the individual products or parts pointing
downwards.
During the adjustment procedures, always pay attention to the OR table and ac-
cessories and avoid collisions. Ensure that tubes, cables and drapes are not
trapped.
W ARNING!
Risk of injury!
Products / accessories not attached properly may loosen and cause injuries.
Always ensure that all locking elements (offset lever, setting clamps, catchs etc.)
of the product / accessory are closed and movable parts are fixed properly. Check
locking after every adjustment procedure.
C AUTION!
Property damage!
Side rail accessories with long lever arms may damage the product.
Never use accessories with long lever arms.
20
1433.01XX
GA 1433.01 EN 08
Basic safety instructions
Safety notes regarding the use of accessories
C AUTION!
Property damage!
If accessories which are mounted to the side rail extend laterally beyond the side
rail near the table top articulations, the table top may collide with the accessories
when making table top adjustments.
When mounting accessories, be sure to observe that the accessory does not
extend laterally beyond the side rail near the table top articulations.
C AUTION!
Property damage!
Using accessories with release levers pointing downwards may cause a collision
with the traction bars during adjustment.
Observe the adjustment procedure carefully and avoid collisions.
2
1433.01XX
GA 1433.01 EN 08
21
Basic safety instructions
2
Safety notes regarding padding
2.4Safety notes regarding padding
D ANGER!
The patient may slip off the table if the padding is not secured properly.
Do not use padding if the Velcro straps on the padding do not line up with the
strips on the product.
Only apply padding to the product that has been authorised for use.
D ANGER!
The patient can slip off the table if the padding is not properly secured.
Worn, loose or wet loop strips will not secure the padding properly on the product.
When attaching the padding, check to ensure that it is properly affixed.
W ARNING!
Health hazard!
In the interests of hygiene the padding must be covered with sterile drapes.
C AUTION!
Property damage!
Padding may be deformed as a result of improper storage.
Padding should only stored flat.
C AUTION!
Improper use can cause property damage!
Use both hands to remove the padding.
22
1433.01XX
GA 1433.01 EN 08
Loading...
+ 130 hidden pages
You need points to download manuals.
1 point = 1 manual.
You can buy points or you can get point for every manual you upload.