Fluke 6000D Impulse Getting Started User Manual

PN 3028662

Getting Started Manual

August 2007

© 2007 Fluke Corporation, All rights reserved. Printed in USA
All product names are trademarks of their respective companies.

Impulse 6000D

Defibrillator Analyzer

Impulse 7000DP

Defibrillator/Transcutaneous Pacer 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 2007, 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- 648-7952 or 1-425-446-6945.

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

In the U.S.A.:
Cleveland Calibration Lab
Tel: [phone]
Email: [e-mail]

Everett Calibration Lab
Tel: 1-888-99 FLUKE (1-888-993-5853)
Email: [e-mail]

In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel: [phone]
Email: [e-mail]

In Asia:
Everett Calibration Lab
Tel: [phone]
Email: [e-mail]

or

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 Impulse 6000D and 7000DP Defibrillator/Transcutaneous Pacer Analyzers are manufactured at Fluke Biomedical, 6920 Seaway Blvd.,
Everett, WA, U.S.A.

Table of Contents

Title Page

Introduction .................................................................................................................... 1

Intended Use.................................................................................................................. 1

Unpacking the Analyzer ................................................................................................. 1

Safety Information .......................................................................................................... 2

Instrument Familiarization .............................................................................................. 4

Turning the Analyzer On ................................................................................................ 7

Connecting a Defibrillator and Pacer to the Analyzer..................................................... 7

Accessing the Analyzer Tests ........................................................................................ 8

What to Do Next............................................................................................................. 12

Maintenance................................................................................................................... 12

Cleaning the Analyzer ............................................................................................... 12

Maintaining Peak Battery Condition........................................................................... 12

Accessories.................................................................................................................... 13

Specifications ................................................................................................................. 14

General Specifications............................................................................................... 14

Defibrillator Analyzer Specifications .......................................................................... 15

Energy Output Measurement................................................................................ 15

i

Impulse 6000D, 7000DP

Getting Started Manual

ECG Waves ......................................................................................................... 17

Transcutaneous Pacemaker Analyzer Specifications (Impulse 7000DP only).......... 22

Test Load Selections............................................................................................ 22

Measurements...................................................................................................... 22

Demand and Asynchronous Mode Test ............................................................... 23

Sensitivity Test ..................................................................................................... 24

Refractory Period Tests........................................................................................ 24

ii

List of Tables

Table Title Page

1. Symbols................................................................................................................................. 2

2. Top-Panel Controls and Connections.................................................................................... 5

3. Rear-Panel Connections ....................................................................................................... 7

4. Accessories ........................................................................................................................... 13

iii

Impulse 6000D, 7000DP

Getting Started Manual

iv

List of Figures

Figure Title Page

1. Top-Panel Controls and Connections.................................................................................... 4

2. Rear-Panel Connections ....................................................................................................... 6

3. Analyzer Ready Display ........................................................................................................ 7

4. Defib Function Menu ............................................................................................................. 8

5. Cursor Navigation Example................................................................................................... 8

6. Defibrillator Connections ....................................................................................................... 9

7. Pacer Connections ................................................................................................................ 11

8. ECG Connections.................................................................................................................. 11

v