Fluke Biomedical warrants this instrument against defects in materials and workmanship for one year from the date of
original purchase OR two years if at the end of your first year you send the instrument to a Fluke Biomedical service center
for calibration. You will be charged our customary fee for such calibration. During the warranty period, we will repair or at our
option replace, at no charge, a product that proves to be defective, provided you return the product, shipping prepaid, to
Fluke Biomedical. This warranty covers the original purchaser only and is not transferable. The warranty does not apply if the
product has been damaged by accident or misuse or has been serviced or modified by anyone other than an authorized
Fluke Biomedical service facility. NO OTHER WARRANTIES, SUCH AS FITNESS FOR A PARTICULAR PURPOSE, ARE
EXPRESSED OR IMPLIED. FLUKE SHALL NOT BE LIABLE FOR ANY SPECIAL, INDIRECT, INCIDENTAL OR
CONSEQUENTIAL DAMAGES OR LOSSES, INCLUDING LOSS OF DATA, ARISING FROM ANY CAUSE OR THEORY.
This warranty covers only serialized products and their accessory items that bear a distinct serial number tag. Recalibration
of instruments is not covered under the warranty.
This warranty gives you specific legal rights and you may also have other rights that vary in different jurisdictions. Since
some jurisdictions do not allow the exclusion or limitation of an implied warranty or of incidental or consequential damages,
this limitation of liability may not apply to you. If any provision of this warranty is held invalid or unenforceable by a court or
other decision-maker of competent jurisdiction, such holding will not affect the validity or enforceability of any other provision.
7/07
Notices
All Rights Reserved
Copyright 2008 2013, Fluke Biomedical. No part of this publication may be reproduced, transmitted, transcribed, stored in a retrieval system,
or translated into any language without the written permission of Fluke Biomedical.
Copyright Release
Fluke Biomedical agrees to a limited copyright release that allows you to reproduce manuals and other printed materials for use in service
training programs and other technical publications. If you would like other reproductions or distributions, submit a written request to Fluke
Biomedical.
Unpacking and Inspection
Follow standard receiving practices upon receipt of the instrument. Check the shipping carton for damage. If damage is found, stop unpacking
the instrument. Notify the carrier and ask for an agent to be present while the instrument is unpacked. There are no special unpacking
instructions, but be careful not to damage the instrument when unpacking it. Inspect the instrument for physical damage such as bent or
broken parts, dents, or scratches.
Technical Support
For application support or answers to technical questions, either email techservices@flukebiomedical.com or call 1-800- 648-7952 or 1-425446-6945.
Claims
Our routine method of shipment is via common carrier, FOB origin. Upon delivery, if physical damage is found, retain all packing materials in
their original condition and contact the carrier immediately to file a claim. If the instrument is delivered in good physical condition but does not
operate within specifications, or if there are any other problems not caused by shipping damage, please contact Fluke Biomedical or your local
sales representative.
Standard Terms and Conditions
Refunds and Credits
Please note that only serialized products and their accessory items (i.e., products and items bearing a distinct serial number tag) are
eligible for partial refund and/or credit. Nonserialized parts and accessory items (e.g., cables, carrying cases, auxiliary modules, etc.)
are not eligible for return or refund . Only products returned within 90 days from the date of original purchase are eligible for refund/credit. In
order to receive a partial refund/credit of a product purchase price on a serialized product, the product must not have been damaged by the
customer or by the carrier chosen by the customer to return the goods, and the product must be returned complete (meaning with all manuals,
cables, accessories, etc.) and in “as new” and resalable condition. Products not returned within 90 days of purchase, or products which are not
in “as new” and resalable condition, are not eligible for credit return and will be returned to the customer. The Return Procedure (see below)
must be followed to assure prompt refund/credit.
Restocking Charges
Products returned within 30 days of original purchase are subject to a minimum restocking fee of 15 %. Products returned in excess
of 30 days after purchase, but prior to 90 days, are subject to a minimum restocking fee of 20 %. Additional charges for damage and/or
missing parts and accessories will be applied to all returns.
Return Procedure
All items being returned (including all warranty-claim shipments) must be sent freight-prepaid to our factory location. When you return an
instrument to Fluke Biomedical, we recommend using United Parcel Service, Federal Express, or Air Parcel Post. We also recommend that
you insure your shipment for its actual replacement cost. Fluke Biomedical will not be responsible for lost shipments or instruments that are
received in damaged condition due to improper packaging or handling.
Use the original carton and packaging material for shipment. If they are not available, we recommend the following guide for repackaging:
Use a double–walled carton of sufficient strength for the weight being shipped.
Use heavy paper or cardboard to protect all instrument surfaces. Use nonabrasive material around all projecting parts.
Use at least four inches of tightly packed, industry-approved, shock-absorbent material around the instrument.
Returns for partial refund/credit:
Every product returned for refund/credit must be accompanied by a Return Material Authorization (RMA) number, obtained from our Order
Entry Group at 1-800-648-7952 or 1-425-446-6945.
Repair and calibration:
To find the nearest service center, go to www.flukebiomedical.com/service or
In the U.S.A.:
Cleveland Calibration Lab
Tel: 1-800-850-4606
Email: globalcal@flukebiomedical.com
In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel: +31-402-675300
Email: ServiceDesk@fluke.com
In Asia:
Everett Calibration Lab
Tel: +425-446-6945
Email: service.international@fluke.com
Certification
This instrument was thoroughly tested and inspected. It was found to meet Fluke Biomedical’s manufacturing specifications when it was
shipped from the factory. Calibration measurements are traceable to the National Institute of Standards and Technology (NIST). Devices for
which there are no NIST calibration standards are measured against in-house performance standards using accepted test procedures.
WARNING
Unauthorized user modifications or application beyond the published specifications may result in electrical shock hazards or improper
operation. Fluke Biomedical will not be responsible for any injuries sustained due to unauthorized equipment modifications.
Restrictions and Liabilities
Information in this document is subject to change and does not represent a commitment by Fluke Biomedical. Changes made to the
information in this document will be incorporated in new editions of the publication. No responsibility is assumed by Fluke Biomedical
for the use or reliability of software or equipment that is not supplied by Fluke Biomedical, or by its affiliated dealers.
Manufacturing Location
The ESA612 Electrical Safety Analyzer is manufactured at Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A.
The Fluke Biomedical ESA612 Electrical Safety Analyzer
(hereafter the Analyzer) is a full-featured, compact,
portable analyzer, designed to verify the electrical safety
of medical devices. The Analyzer tests to domestic
(ANSI/AAMI ES1, NFPA 99) and international (IEC62353,
AN/NZS 3551, and parts of IEC 60601-1) electrical-safety
standards. The integrated ANSI/AAMI ES1 and
IEC60601-1 patient loads are easily selectable.
The Analyzer performs the following tests:
• Line (Mains) voltage
• Ground Wire (or Protective Earth) Resistance
• Equipment current
• Insulation resistance
• Ground (Earth) leakage
• Chassis (Enclosure) leakage
• Lead to Ground (Patient) and Lead to Lead (Patient
Auxiliary) leakage
• Lead isolation (Mains on applied parts leakage)
• Differential leakage
• Direct equipment leakage
• Direct applied part leakage
• Alternative equipment leakage
• Alternative applied part patient leakage
• Point to point leakage, voltage, and resistance
• ECG simulation and performance waveforms
1
ESA612
Users Manual
Table 1. Symbols
Symbol Description
Important information; refer to manual.
Hazardous voltage
Conforms to relevant Canadian and US standards
Conforms to relevant Australian EMC requirements
Conforms to European Union directives
This product complies with the WEEE Directive (2002/96/EC) marking requirements. The affixed label
indicates that you must not discard this electrical/electronic product in domestic household waste. Product
CAT II
2
Category: With reference to the equipment types in the WEEE Directive Annex I, this product is classed as
category 9 "Monitoring and Control Instrumentation" product. Do not dispose of this product as unsorted
municipal waste. Go to Fluke’s website for recycling information.
IEC Measurement Category II – CAT II equipment designed to protect against transients from energyconsuming equipment supplied from fixed installations.
Accessible Functional Earth Terminal
Electrical Safety Analyzer
Safety Information
Safety Information
In this manual, a Warning identifies hazardous conditions
and actions that could cause bodily harm or death. A
Caution identifies conditions and actions that could
damage the Analyzer, the equipment under test, or cause
permanent loss of data.
Warning
To avoid possible electrical shock or
personal injury, follow these guidelines:
• Use this Analyzer only in the manner
specified by the manufacturer or the
protection provided may be impaired.
• Read the Users Manual before operating
the Analyzer.
• Do not connect the Analyzer to a patient or
equipment connected to a patient. The
Analyzer is intended for equipment
evaluation only and should never be used
in diagnostics, treatment or in any other
capacity where the Analyzer would come
in contact with a patient.
• Do not use the product in wet or damp
locations, around explosive gases or dust.
• Inspect the Analyzer before using it. Do
not use the Analyzer if abnormal
conditions of any sort are noted (such as a
faulty display, broken case, etc.)
• Inspect the test leads for damaged
insulation or exposed metal. Check test
lead continuity. Replace damaged leads
before using the Analyzer.
• When testing, always be sure to keep your
fingers behind the safety barriers on the
test leads.
• Never open the Analyzer's c ase.
Dangerous voltages are present. There are
no user replaceable parts in the Analyzer.
• Have the Analyzer serviced on l y by
qualified personnel.
3
ESA612
Users Manual
• The Analyzer must be properly earthed.
Only use a supply socket that has a
protective earth contact. If there is any
doubt as to the effectiveness of the supply
socket earth, do not connect the Analyzer.
Do not use a two-conductor adapter or
extension cord; this will break the
protective ground connection.
• Do not use the 15-20 A adapter to power
devices rated in excess of 15 A. Doing so
may overload the installation.
• Use extreme caution when working with
voltages above 30 V.
• Use the proper terminals, functions and
ranges for the test being performed.
• Do not touch metal parts of the device
under test (DUT) during analysis. The DUT
should be considered an electrical shock
hazard when connected to the Analyzer as
some tests involve high voltages, high
currents, and/or the removal of DUT earth
bond.
Intended Use
The Product is an electronic signal source and
measurement device for verifying the electrical safety of
medical devices. The Product also provides ECG
simulation and performance waveforms to verify patient
monitors are performing within their operating
specifications.
The Product provides the following function categories:
• ECG Functions
• ECG-Performance Testing
4
Electrical Safety Analyzer
Unpacking the Analyzer
The intended user is a trained biomedical equipment
technician who performs periodic preventative
maintenance checks on patient monitors in service. Users
can be associated with hospitals, clinics, original
equipment manufacturers and independent service
companies that repair and service medical equipment.
The end user is an individual, trained in medical
instrumentation technology.
This Product is intended to be used in the laboratory
environment, outside of the patient care area, and is not
intended for use on patients, or to test devices while
connected to patients. This Product is not intended to be
used to calibrate medical equipment. It is intended for
over-the-counter use.
Unpacking the Analyzer
Carefully unpack all items from the box and check that
you have the following items:
• ESA612
• Getting Started Manual
• Users Manual CD
• Carrying case
• Power cord
• 15 – 20 A Adapter (USA only)
• ESA USA Accessory Kit (USA, Australia, and Israel
only)
• ESA EUR Accessory Kit
• Ansur demo CD
• Null Post Adapter
• 5-to-5 Banana to ECG Adapter (BJ2ECG)
• Transfer cable
5
ESA612
Users Manual
Instrument Familiarization
Figure 1 and Table 2 describes the front-panel controls
and connections of the Analyzer.
1
9
2
8
TEST
7
Figure 1. Front-Panel Controls and Connections
3
4
5
6
fis116.eps
Table 2. Top-Panel Controls and Connections
Item Name Description
Controls the configuration of
Equipment Outlet
Configuration
1
Buttons
the equipment outlet. Opens
and closes the neutral and
ground connection and
reverses the polarity of the
neutral and hot connection.
Indicates when high voltage
High Voltage
2
Indicator
is applied to the
ECG/Applied Parts posts or
L1 and L2 of the Test
Receptacle.
Test Function
3
Buttons
Navigation Buttons
4
Selects the various Analyzer
test functions.
Cursor control buttons for
navigating menus and lists.
6
Electrical Safety Analyzer
Instrument Familiarization
Item Name Description
Test Button
5
Save Button
6
Input Jacks
7
Nulling Jack
8
Function Softkeys
9
Initiates selected tests.
Saves the measurement or
ECG waveform to memory.
Test lead connectors.
Connection for zeroing test
lead resistance.
Keys F1 through F4 are used
to select from a number of
selections that appear in the
LCD display above each
function softkey.
7
ESA612
Users Manual
Figure 2 and Table 3 describe the side and top-panel connections of the Analyzer.
RA
RFLNC1
LLLARL
V1
R
RA
FLN
LLLARL
C1
V1
TEST
1
3
*Old versions have a B style connector for USB port.
Figure 2. Side and Top-Panel Connections
8
Old Version*
7
4
2
9
8
5
6
fis110.eps
Electrical Safety Analyzer
Instrument Familiarization
Table 3. Side and Top-Panel Connections
Item Name Description
1 Equipment Outlet
USB Device Port
2
(Mini B-style connector)1
3 Fuse Access Door Covers the equipment outlet fuses.
4 Tilt Stand Support for holding the Analyzer in a tilted position.
5 AC Power Switch Turns ac power on and off.
6 Power Input Connector
7 ECG/Applied Parts Jacks
8 Banana Jack to ECG Adapter Adapter for connecting ECG snap leads to the Analyzer.
9 Carry Handle
1 Older versions of the Analyzer have a B-style USB port connector.
Equipment outlet, specific to the version of the Analyzer, which provides a DUT
connection.
Digital connection for controlling the Analyzer from a PC or instrument
controller.
A grounded male three-prong (IEC 60320 C19) connector that accepts the
line-power cord.
Connection posts for Device Under Test (DUT) applied parts, such as ECG
leads. Used to test for leakage current through leads and to supply ECG
signals and performance waveforms to a DUT.
Handle to transport Analyzer. Note: There is no handle on old versions of the
analyzer.
9
ESA612
Users Manual
How to Hold the Product
When you move the Analyzer, use the handle in the
bottom case to hold it. See Figure 3.
Note
There is no handle on old versions of the
Analyzer.
Figure 3. Product Handle
fis122.eps
Connecting to Line Power
Warning
To avoid shock hazard and for proper
Analyzer operation, connect the factory
supplied three-conductor line power cord to
a properly grounded power outlet. Do not
use a two-conductor adapter or extension
cord; this will break the protective ground
connection.
Connect the Analyzer to a properly grounded three-prong
outlet. The Analyzer will not properly test a DUT when the
ground lead is open.
The Analyzer is intended for use with single-phase,
grounded power. It is not intended for dual, split-phase or
three-phase power configurations. But it can be used with
any power system that supplies the correct voltages for
single-phase and is grounded, or is an isolated power
system.
10
Electrical Safety Analyzer
Connecting a DUT to the Analyzer
Connecting a DUT to the Analyzer
A Device Under Test (DUT) can be connected in a
number of different ways depending on the device and
the number of connections needed for a full electrical
safety test. Figure 5 shows a DUT connected to the test
receptacle, applied parts posts, and a separate
connection to the DUT’s enclosure or protective earth
ground.
Turning the Analyzer On
Note
To ensure the high voltage indicator is working,
look for it to illuminate during the power-up self
test.
Press the power switch on the left-side panel so the “I”
side of the ac power switch is depressed. The Analyzer
will perform a series of self tests and then display the
message shown in Figure 4 when the self test has
completed successfully.
Figure 4. Analyzer Ready for Operation
fis101.jpg
11
ESA612
Users Manual
Connect ESA612
to grounded
mains socket.
To protective earth or
any exposed conductive
surface on the enclosure
RA
R
LL
F
LA
L
RL
N
V1
C1
TEST
Connect the DUT ac power cord to the
equipment outlet on the Analyzer
12
Figure 5. DUT Connections to the Analyzer
fis113.eps
Electrical Safety Analyzer
Accessing the Analyzer’s Functions
During the self-test, the Analyzer checks its ac mains
input for proper polarity, ground integrity and voltage
level. The high voltage indicator illuminates briefly during
the self test. If the polarity is reversed, the Analyzer
indicates this condition and allows the polarity to be
reversed internally. If the ground is open, the Analyzer
displays this fault. If the mains voltage is too high or too
low, the Analyzer displays this fault and does not continue
until the supply voltage is corrected and the Analyzer
power cycled off and then on again.
Accessing the Analyzer’s Functions
For each test and setup function, the Analyzer uses a
series of menus to access various Analyzer test and
setup variables. As shown in Figure 6, the Analyzer
indicates various leakage current tests along the bottom
of the display. An Exit selection is also indicated as a way
of backing out of the leakage current tests. Pressing a
softkey (F1 through F4) under a specific test will cause
the analyzer to setup for or perform the selected test.
In addition to the function softkeys, the Analyzer test
functions may require using the navigation buttons to
select parameters as well. In the example above, the
leakage selection has next to it. This icon indicates the
selection is controlled by pressing or . In this
example, the leakage current measurement is switched
between AC+DC, AC only, or DC only. The applied parts
indicator has on the left end and on the right end.
These icons indicate the use of and to select an
applied part.
fis102.jpg
Figure 6. Leakage Current Menu
The three buttons along the right side of the display
() control the wiring of the Analyzer’s
test receptacle for some electrical tests. The present state
of these three buttons is displayed along the right edge of
the display whenever these controls are active.
13
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