Fluke QA-ES III Parts list manual

PN 4473063
December 2015, Rev. 1
© 2015 Fluke Corporation. All rights reserved. Specifications are subject to change without notice.
All product names are trademarks of their respective companies.
QA-ES III
Electrosurgery Analyzer

Warranty and Product Support
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 2015, 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 techservice[email protected] or call 1-800- 850-4608 or 1-440-
248-9300. In Europe, email [e-mail] or call [phone].
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.

Returns and Repairs
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 1-440-498-2560.
Repair and calibration:
To find the nearest service center, go to www.flukebiomedical.com/service or
In the U.S.A. and Asia:
Cleveland Calibration Lab
Tel: [phone] x2564
Email: [email protected]
In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel: [phone]
Email: [email protected]
To ensure the accuracy of the Product is maintained at a high level, Fluke Biomedical recommends the product be calibrated at least
once every 12 months. Calibration must be done by qualified personnel. Contact your local Fluke Biomedical representative for
calibration.

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 QA-ES III Electrosurgery Analyzer is manufactured at Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A.

i
Table of Contents
Title Page
Introduction .................................................................................................................... 1
Intended Use.................................................................................................................. 1
Safety Information .......................................................................................................... 2
Terminology ................................................................................................................... 5
Unpack the Product........................................................................................................ 5
Product Familiarization................................................................................................... 5
Turn On the Product....................................................................................................... 8
Top Menus ..................................................................................................................... 8
Measurement Connections ............................................................................................ 10
Footswitch Connections ............................................................................................ 10
Neutral Connections.................................................................................................. 10
Setup Communications .................................................................................................. 11
USB Device Port........................................................................................................ 11
Windows Software Driver ..................................................................................... 11
Device Manager.................................................................................................... 12

QA-ES III
Getting Started Manual
ii
Wireless Port............................................................................................................. 13
Product Maintenance..................................................................................................... 14
Cleaning.................................................................................................................... 15
Troubleshooting ........................................................................................................ 15
Replaceable Parts..................................................................................................... 15
Accessories .............................................................................................................. 16
General Specifications................................................................................................... 16
Technical Specifications ................................................................................................ 17

1
Introduction
The QA-ES III (or the Product) measures the
performance of high frequency Electrosurgery Units
(ESU) and saves test records that you can transmit to a
computer (PC). You can control the Product remotely
from the Fluke Ansur software program.
The Product makes these measurements and tests:
•Generator output:
οPower, RMS
οCurrent, RMS
οVoltage, peak-to-peak
οCrest Factor
•Vessel Sealing Loop Current
•HF Leakage Current in various configurations
•Contact Quality Monitor (CQM) test
•Power Distribution test automatically makes a series
of Generator Output measurements at various loads
Intended Use
The Product is a precision instrument for use in
performing tests on high-frequency electrosurgical units in
accordance with national and international standards. It is
for use by trained service technicians. Tests include
automatic power distribution measurement, crest factor
measurement, RF leakage measurement, and CQM
(contact quality monitor) test. The Product will be used in
hospitals, clinical engineering departments, independent
service organizations, and at ESU OEMs. The Product
will not be used in patient rooms while a patient is
present.

QA-ES III
Getting Started Manual
2
Safety Information
A Warning identifies conditions and procedures that are
dangerous to the user. A Caution identifies conditions
and procedures that can cause damage to the Product or
the equipment under test.
Table 1 is a list of symbols used on the Product or in this
manual.
Table 1. Symbols
Symbol Description
WRisk of Danger. Important information. See Manual.
XHazardous voltage. Risk of electric shock.
PConforms to European Union directives.
)Conforms to relevant North American Safety Standards.
Conforms to relevant Australian EMC standards.
~
This product complies with the WEEE Directive marking requirements. The affixed label indicates that you
must not discard this electrical/electronic product in domestic household waste. Product 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.

Electrosurgery Analyzer
Safety Information
3
XW Warning
To prevent possible electrical shock, fire, or
personal injury, follow these guidelines:
•Read all safety information before you
use the Product.
•Use the Product only as specified, or the
protection supplied by the Product can
be compromised.
•Limit operation to the specified
measurement category, voltage, or
amperage ratings.
•Use the correct terminals, function, and
range for measurements.
•Carefully read all instructions.
•Do not touch voltages >30 V ac rms,
42 V ac peak, or 60 V dc.
•Do not use the Product around explosive
gas, vapor, or in damp or wet
environments.
•Do not use the Product if it operates
incorrectly.
•Examine the case before you use the
Product. Look for cracks or missing
plastic. Carefully look at the insulation
around the terminals.
•Do not use test leads if they are
damaged. Examine the test leads for
damaged insulation, exposed metal, or if
the wear indicator shows. Check test
lead continuity.
•Use this Product indoors only.
•Use only the mains power cord and
connector approved for the voltage and
plug configuration in your country and
rated for the Product.
•Make sure the ground conductor in the
mains power cord is connected to a
protective earth ground. Disruption of
the protective earth could put voltage on
the chassis that could cause death.
•Replace the mains power cord if the
insulation is damaged or if the insulation
shows signs of wear.

QA-ES III
Getting Started Manual
4
•Use only current probes, test leads, and
adapters supplied with the Product.
•Connect the common test lead before
the live test lead and remove the live test
lead before the common test lead.
•Only use probes, test leads, and
accessories that have the same
measurement category, voltage, and
amperage ratings as the Product.
•Remove all probes, test leads, and
accessories that are not necessary for
the measurement.
•Do not connect measurement inputs
directly to mains.
•Do not use test leads if they are
damaged. Examine the test leads for
damaged insulation and measure a
known voltage.
•Disable the Product if it is damaged.
•Do not use the Product if it is damaged.
•Do not touch exposed metal on banana
plugs, they can have voltages that could
cause death.
•Remove circuit power before you
connect the Product in the circuit when
you measure current. Connect the
Product in series with the circuit.
•Connect an approved three-conductor
mains power cord to a grounded power
outlet.
•Do not put the Product where access to
the mains power cord is blocked.
•Make sure that the Product is grounded
before use.
•Do not put metal objects into
connectors.
•Make sure that the space around the
Product meets minimum requirements.
•Do not use the Analyzer in CAT II, III, or
IV environments.
•Retractable end of test leads are for use
on ESU only.
•No probes or accessories supplied with
the Analyzer are intended for handheld
use. Setup and stand clear when
activating the ESU with the footswitch.

Electrosurgery Analyzer
Terminology
5
Terminology
The Product uses the following terminology as described
in IEC 60601-2-2:
•HF – high frequency surgical signals also called RF
(radio frequency).
•Neutral Electrode also called Dispersive Electrode.
•Contact Quality Monitor (CQM) also called Return
Electrode Monitor (REM trademarked by Covidien)
or Return Electrode Current Monitor (RECM).
Unpack the Product
Carefully unpack all items from the box and check that
you have the following items:
•QA-ES III Electrosurgery Analyzer
•Users Manual on CD
•Getting Started Manual
•Alligator clips, black and red
•Dispersive safety lead
•CQM safety lead
•Jumper safety lead (Shorting Leads)
•40 inch stackable/retractable safety leads, black, red
(2), blue, yellow, and green
•20 inch stackable/retractable safety leads, black and
red
•Multi-stacking 4 mm banana plug patch cord, black
•RECM Alarm Disabling Lead
•Bipolar Activation Lead
•USB cable
•Ansur Software CD ROM
Product Familiarization
Figure 1 and Table 2 describe the controls and
connections on the product.

QA-ES III
Getting Started Manual
6
ELECTROSURGERY ANALYZER
QA-ES III
CUT COAG
COMMON CQM
VARIABLE HI VARIABLE LO
FIXED FIXED F1
BACK USB
F2 F3 F4 F5
SWITCHES
LOADS
5kV PEAK
400W MAX
1245
6
7
8
3
9
10
11
11
12
hwg001.eps
Figure 1. Product Controls and Connections

Electrosurgery Analyzer
Product Familiarization
7
Table 2. Controls and Connections
Item Description
Footswitch connections: CUT, COAG, COMMON
CQM connection for the Contact Quality Monitor test
Load connections: VARIABLE HI, VARIABLE LO, FIXED
LCD
Rotary selector knob
USB Device port
Function keys (F1 through F5)
BACK key
Scope out
Mains power connection and On/Off switch
Bumpers to protect back panel
Ground lug

QA-ES III
Getting Started Manual
8
Turn On the Product
Before you turn on the Product, check for damage or
wear. Check for adequate ventilation. The Product
requires a clear area of 10 cm (4 in) at the rear panel and
all vent openings.
Connect the power cord to Mains power and push the
power switch. The start-up sequence begins.
During the start-up sequence, a screen shows the
firmware version for reference. You can use the start-up
sequence to update the firmware.
After the start-up sequence, the Product starts the
application. When the Top Menu screen shows, the
Product is ready for use.
Top Menus
The Top Menus 1 and 2 have sub-menus to make
measurements, set up the instrument, and maintain
memory. Use the controls and softkeys to make
selections from the menus. Table 3 describes the Top
Menu controls.
For complete operating instructions, refer to the Users
Manual on the accompanying CD. Manuals are also
available at www.flukebiomedical.com.

Electrosurgery Analyzer
Top Menus
9
Table 3. Top Menu Controls
hwg002.eps hwg003.eps
Softkey Goes to Softkey Goes to
F1 Generator Output measurement menu F1 Power Distribution measurement menu
F2 Vessel Sealing measurement menu F2 --
F3 HF Leakage measurement menu F3 Memory menu
F4 CQM (Contact Quality Monitor) test menu F4 Clock menu
F5 Top Menu 2 for more functions F5 --
Note
Use the BACK key to return to Top Menu 1.

QA-ES III
Getting Started Manual
10
Measurement Connections
Connect the ESU to the Product to make measurements.
See the Users Manual for more information.
Footswitch Connections
Some ESUs use a footswitch to turn on the ESU
generator. The Product has connections that simulate a
footswitch. Use the footswitch feature to automatically
turn on the ESU generator at an appropriate time.
Note
As an alternative to a footswitch, some ESUs
use a hand switch. For this manual, hand
switches and footswitches are both called
footswitches.
It is not practical to make a single measurement or a
Power Distribution test without the footswitch feature.
Without the feature, you must manually turn on the ESU
(or use an actual footswitch or hand switch) at the correct
time after the delay starts.
The Product has connections for both CUT (yellow) jack
and COAG (blue) jack footswitches and a COMMON
(gray) connection jack.
The footswitch feature is available during all
measurements and CQM tests. In continuous
measurement mode, the Product activates the footswitch
relays to turn on the ESU. The ESU remains on and the
footswitch is engaged until you stop the measurement.
If you are not using the footswitch feature, ignore the
footswitch connections.
Neutral Connections
ESUs with CQM alarms have two neutral connections.
You must connect the neutral connections together for
Generator Output, Vessel Sealing, and HF Leakage
measurements.
The Shorting Leads supplied with the Product have a
resistance that is sufficiently low to prevent an alarm on
the ESU. Some ESUs require the Shorting Lead to have
a minimum resistance, as well as, a maximum resistance.
A simple jumper may not work. Use the Shorting Leads
for all measurements except the CQM test.

Electrosurgery Analyzer
Setup Communications
11
Setup Communications
The Product has a USB Device Port for communication to
a computer (PC). Some Products also have wireless
functionality. You can use the communications ports to:
•Send saved test records to a PC.
•Send commands and receive responses to control
the Product remotely.
Use Ansur or a terminal emulation program (for example
HyperTerminal or Tera Term) to set the COM port
options. COM port settings are:
•115,200 baud
•No parity
•8 data bits
•1 stop bit
•Hardware handshaking is on. (The Product uses
hardware handshaking but does not use XON/XOFF
software handshaking.)
Operating system requirements:
•Windows Vista
•Windows 7
•Windows 8 or later
USB Device Port
The USB port on the Product (a Micro Type B connector)
connects to a USB controller port on the PC (Type A
rectangular connector). Use the supplied USB Type A-to-
Micro-B cable to connect the Product to a PC.
The PC sees the USB Port while the cable is connected
to the Product (even if the Product is turned off). If the
cable is disconnected, the PC must close the port and
reopen the connection.
Windows Software Driver
The USB port uses an integrated circuit (IC) to convert
USB to RS232. Adapter cables frequently use this IC
(FT232R from the company FTDI). When the Product
connects to a PC for the first time, the PC registers the
Product as a virtual COM port (VCP). The virtual COM
port looks like a serial (RS232) device.
The IC is compatible with the USB Version 2.0 Full Speed
specification. The USB ID numbers are: VID 0403 and
PID 6001.

QA-ES III
Getting Started Manual
12
Device Manager
The Device Manager is a PC program that changes COM
port settings. Access the Device Manager according to
your operating system, usually one of these methods:
•From the Control Panel, select Device Manager.
•Select Hardware and Sound and then select
Device Manager (under Devices and Printers).
Table 4 describes the functions of the Device Manager.
Note
While the Device Manager on the PC can set
COM port options, the controlling program
overwrites the Device Manager settings.
Table 4. COM Port Controls
Function Steps
Enable the
driver
1. Right-click USB Serial
Converter and select
Properties | Advanced.
2. Select Load VCP and click OK.
3. Click OK. The COM port shows
in the Device Driver.
Table 4. COM Port Controls (cont.)
Function Steps
Verify COM port
settings
1. Right-click the COM port.
2. Select Port Settings and
check the settings.
Change the
COM port
number
assigned by
Windows:
1. Right-click the USB Serial Port
(COMx) and select Properties
| Port Settings | Advanced.
2. Select the number from the
COM Port Number menu and
click OK.
3. Scan for hardware changes.
The device list shows the new
COM port number.
If the COM port number is in use,
the number could be assigned to
an unused device. Click through
the error message to use the
number.