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.