Fluke QA-ES III User 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 [e-mail] or call 1-800- 850-4608 or 1-440­248-9300. 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: [e-mail]

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.

In Europe, Middle East, and Africa:
Eindhoven Calibration Lab

Tel: [phone]
Email: [e-mail]

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.

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

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QA-ES III

Getting Started Manual

Wireless Port............................................................................................................. 13

Product Maintenance ..................................................................................................... 14

Cleaning .................................................................................................................... 15

Troubleshooting ........................................................................................................ 15

Replaceable Parts ..................................................................................................... 15

Accessories .............................................................................................................. 16

General Specifications ................................................................................................... 16

Technical Specifications ................................................................................................ 17

ii

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:
ο Power, RMS
ο Current, RMS
ο Voltage, peak-to-peak
ο Crest 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.

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QA-ES III

Getting Started Manual

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. Symbols

Symbol Description

Table 1 is a list of symbols used on the Product or in this
manual.

W Risk of Danger. Important information. See Manual.
X Hazardous voltage. Risk of electric shock.
P Conforms 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.

2

Electrosurgery Analyzer

Safety Information

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.

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QA-ES III

Getting Started Manual

• 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.

4

Electrosurgery Analyzer

Terminology

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.

5

QA-ES III

Getting Started Manual

1

SWITCHES

LOADS

5kV PEAK
400W MAX

ELECTROSURGERY ANALYZER

QA-ES III

CUT COAG

COMMON CQM

VARIABLE HI VARIABLE LO

FIXED FIXED

2

4

3

F1

F2 F3 F4 F5

BACK

8

USB

7

Figure 1. Product Controls and Connections

5

12

11

9

10

11

6

hwg001.eps

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Electrosurgery Analyzer

Product Familiarization

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

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QA-ES III

Getting Started Manual

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.

8

Electrosurgery Analyzer

Top Menus

Table 3. Top Menu Controls

hwg002.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 --

Use the BACK key to return to Top Menu 1.

Note

hwg003.eps

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QA-ES III

Getting Started Manual

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.

10

Electrosurgery Analyzer

Setup Communications

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

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-to­Micro-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.

• Windows 8 or later

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QA-ES III

Getting Started Manual

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

1. Right-click USB Serial
Converter and select

Enable the
driver

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

Change the
COM port
number
assigned by
Windows:

1. Right-click the COM port.

2. Select Port Settings and

check the settings.

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.

12

Electrosurgery Analyzer

Setup Communications

Wireless Port

For Products with wireless functionality, the wireless port
communicates with a PC that has an 802.15 (Bluetooth)
wireless interface. For PCs without the interface, use a
commercially available USB adapter. The PC starts the
interface when you connect the adapter. (Additional
software is not necessary.)

The PC sees the wireless port while the Product is on.
When the Product is turned off, the PC closes the port.
When the wireless device is assigned to a COM port, the
COM port reopens when the Product is turned on again.

Note

The wireless port on the Product is a Classic
Bluetooth port not a Low Energy Bluetooth port.

To install a wireless device:

1. Right-click the Bluetooth Devices icon and select

Add a Device, or select Show Bluetooth Devices |
Add a Device.

The Product shows in the window. The serial number
of the Product is part of the name.

Note

It is okay if the icon is a headset, or if the name
is Bluetooth headset. These are defaults and the
name will change to the Product.

2. Select the Product and click Next.

The system prompts you to compare the codes.
Ignore the message and continue with the next step.

3. Make sure Yes is selected and click Next.

4. Select Driver Software Installation.

The system installs two standard serial-over­Bluetooth-link COM ports. The Bluetooth Peripheral
Device will fail. Ignore the message and close the
window. The Add a device window shows the device
successfully added to the computer.

5. Close the Add a device window.

6. Right-click the Bluetooth icon and select Show
Bluetooth Devices.

The Product name (including serial number) shows.
Ignore the message about the missing driver for the
Bluetooth Peripheral Device.

7. Right-click the Product and select Properties.
The Hardware section shows a COM port for a

Standard Serial-over-Bluetooth link. Use this
Outgoing COM port for the interface.

The Bluetooth Settings COM ports show that the
Product has 2 COM ports: Outgoing (initiated by the
PC) and Incoming (initiated by the Product). The
system uses the Outgoing port only.

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QA-ES III

Getting Started Manual

Wireless Settings—For Products with wireless
functionality, Table 5 shows the settings. You do not need
to change the default settings. Choose a method to open
Bluetooth settings:

• Right-click the Bluetooth icon and select Open
Settings.

• Right-click Bluetooth from the Start menu.

• If you installed an adapter, select Control Panel |

Devices and Printers, then right-click the adapter
and select Bluetooth Settings.

Table 5. Bluetooth Settings

Option Recommended Setting

Allow Bluetooth devices to
connect to this computer.

Alert me when a new
Bluetooth device wants to
connect.

Show the Bluetooth icon in
the notification area.

Allow Bluetooth devices to
find this computer.

Selected (Required)

Selected

Selected

Not selected (The PC
uses the Outgoing COM
port to find the Product.)

Product Maintenance

XW Warning

To prevent possible electrical shock, fire, or
personal injury, follow these guidelines:

• Do not use an extension cord or adapter
plug.

• Do not operate the Product with covers
removed or the case open. Hazardous
voltage exposure is possible.

• Disconnect the mains power cord and
input cables before you remove the
Product covers.

• Remove the input signals before you
clean the Product.

• Use only specified replacement parts.

• Have an approved technician repair the

Product.

After troubleshooting or maintenance, restart the Product
and ensure that it starts without errors.

For radio frequency certification, see

www.flukebiomedical.com

14

Electrosurgery Analyzer

Product Maintenance

Cleaning

WCaution

For safe operation and maintenance of the
Product:

• Do not spray cleaning solution or water
directly on the Product.

• Do not pour or drip liquid onto the
Product.

The Product needs little maintenance or special care. To
clean, wipe with a damp cloth.

Troubleshooting

Table 6 shows possible problems and solutions.

Table 6. Troubleshooting

Symptom Resolution

The Product does not
show the Top Menu.

The Product fails during
the initial self-test.

Time stamp on saved
records is not accurate.

Ensure the Product is
connected to power.

Contact Fluke Biomedical
Technical support.

Set the clock and then turn
on the Product and keep it
on for a minimum of 1 hour.

Replaceable Parts

Table 7 lists the replaceable parts for the Product.

Table 7. Replaceable Parts

Item

AC285 Large Alligator Clips,
Black, Red

ESU-Dispersive Safety Lead 4635167
ESU-CQM Safety Lead 4635171
ESU-Jumper Safety Lead 2772209

Micro USB cable (2 m) 4114833

40 Inch Safety Leads, Black, Red
(Stackable/Retractable)

40 Inch Blue Safety Lead
(Stackable/Retractable)

40 Inch Yellow Safety Lead
(Stackable/Retractable)

40 Inch Green Safety Lead
(Stackable/Retractable)

Fluke Biomedical

Part Number

1610159

2772159

4635180

4635198

4635209

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QA-ES III

Getting Started Manual

Table 7. Replaceable Parts (cont.)

Item

20 Inch Black Safety Lead
(Stackable/Retractable)

20 Inch Red Safety Lead
(Stackable/Retractable)

Fluke Biomedical

Part Number

4635211

4635227

40 Inch Black Safety Lead (Stackable) 4635230
Multi-stacking 4 mm banana plug

patch cord

4605232

RECM Alarm Disabling Lead 4635253
Bipolar Activation Lead 4635266

Accessories

Table 8 is a list of optional accessories.

Table 8. List of Optional Accessories

Item

International Dispersive Lead (1/4 in
Phono Plug)

Test Probe Set, 0.080 Brass Tip 1909216

Fluke Biomedical

Part Number

4635248

General Specifications

Physical

Housing ............................... Metal case

Size (HxWxL) ...................... 14.5 cm x 35 cm x 47 cm

(5.75 in x 13.75 in x 18.5 in)

Weight ................................. 7.5 kg (16.5 lbs)

Power

Power Requirements .......... 100 V ac, 115 V ac, 230 V ac,

50 Hz / 60 Hz, universal input
100 V/115 V: 20 VA
230 V: 30 VA

User Interface

LCD ..................................... Monochrome 240 pixels x

64 pixels, 8 lines x 40 characters,
white LED backlight

Keys .................................... 6 (1 fixed, 5 soft-defined) and

Rotary selector knob

Environmental Specifications

Temperature

Operating ........................ 10 °C to 40 °C (50 °F to 104 °F)

Storage ........................... -20 °C to 60 °C (-4 °F to 140 °F)

Humidity .............................. 10 % to 90 % non-condensing

Altitude ................................ 2000 m maximum

IP Rating ............................. IEC60529:IP20

Ansur QA-ES MK III Plug-In License 4704312

16

Electrosurgery Analyzer

Technical Specifications

Electromagnetic Compatibility (EMC)

IEC 61326-1: Basic
Emissions

Classification ...................... IEC CISPR11: Group 1, Class A.

Group 1 have intentionally generated and/or use
conductively coupled radio-frequency energy which is
necessary for the internal functioning of the equipment
itself. Class A equipment is suitable for use in non­domestic locations and/or directly connected to a low­voltage power supply network

USA (FCC) ......................... Intentional Radiators

This device complies with part 15 of the FCC Rules.
Operation is subject to the following two conditions: (1)
This device may not cause harmful interference, and (2)
this device must accept any interference received,
including interference that may cause undesired operation.
(15.19)

Changes or modifications not expressly approved by Fluke
could void the user's authority to operate the equipment.
(15.21)

Safety

IEC 61010-1:Overvoltage category II, pollution degree 2
IEC 61010-2-030: Measurement 5,000 V

Wireless Module Listing

FCC (United States) compliant

(Class A)............................. FCC ID: X3ZBTMOD3

IC (Industry Canada)

compliant ............................ IC: 8828A-M OD3

CE (European) certified ...... CE0051

Technical Specifications

Specifications apply for a period of one year from date of the
most recent calibration.

Measures ................................ Cut and coag waveforms

Power and current

measurements ....................... true RMS

Bandwidth ............................. 30 Hz to 5 MHz at -3 dB including

Delay Time for single

measurements ....................... 0.2 seconds to 4.0 seconds from

Duty Cycle

Variable Load ..................... 10 seconds on, 30 seconds off, at

Fixed 200 Ω Load .............. 10 seconds on, 30 seconds off, at

Generator Output Measurements

Load Resistance

Variable ......................... 0 Ω, 10 Ω, 20 Ω, 25 Ω to 2500 Ω

Accuracy ........................ ±2.5 %

Monopolar and bipolar outputs

loads

Foot Switch activation to start of
measurement

100 W, all loads

400 W

(by 25 Ω), 2500 Ω to 5200 Ω (by
100 Ω)

17

QA-ES III

Getting Started Manual

Power

Ranges ............................ 0.0 W to 99.9 W

100 W to 500 W

Accuracy ...................... < 10 W: ±5 % + 1 W

≥10 W: ±5 %

Maximum

At 25% duty cycle (10 seconds on,

30 seconds off) ........... 10 Ω: 300 W,

20 Ω to 2900 Ω: 400 W,
3000 Ω to 5200 Ω: 200 W

At 10% duty cycle (5 seconds on,

45 seconds off) ........... 10 Ω: 300 W,

20 Ω to 2400 Ω: 500 W,
2425 Ω to 2900 Ω: 400 W,
3000 Ω to 5200 Ω: 200 W

Current

RMS ........................... 0 mA to 5,500 mA

Accuracy ..................... ±(2.5 % of reading + 1 mA)

Voltage

Peak .......................... 10 kV Peak to Peak

Accuracy ..................... ±(10 % of reading + 50 V)

Crest Factor ........................ 1.4 to 16.0

Defined as the ratio of Peak voltage to RMS voltage (Vpk /
Vrms), using the larger of the 2 peaks (positive or
negative)

Vessel Sealing Measurement

Loop Current, RMS ............. 0 mA to 5500 mA

Accuracy ............................ ±(2.5 % of reading + 1 mA)

HF Leakage Current

Fixed Load .......................... 200 Ω

Load Accuracy .................... ±2.5 %

Power rating ........................ 400 W

Additional Fixed Load ......... 200 Ω

Current, RMS ...................... 0 mA to 5500 mA

Accuracy ............................. ±(2.5 % of reading + 1 mA)

CQM Test (Contact Quality Monitor)

Resistances ........................ 0 Ω to 475 Ω (by 1 Ω)

Accuracy ............................. 0 Ω to 10 Ω ±0.5 Ω,

11 Ω and above ±5 %

Power rating ....................... 0.5 W

Auto Time interval ............... 1 second to 5 seconds

Oscilloscope Output

1 V per ampere of input current, typical.

Footswitch Simulations

Cut and Coag

Communications

USB Device Port ................. Micro B connector

Full speed

Wireless Port ...................... 802.15, Speed:115,200 baud

Memory

Test Records ...................... 5,000

Non-volatile ........................ retained through power cycling

Calibration

Traceable to the International System of Units (SI) through the
appropriate National Metrology Institutes such as NIST or
through intrinsic standards.

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