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xviii

MAINTENANCE

SECTION 3

Cleaning the WAM Transmitter and ECG Cable ........................................................................................ 19
Periodic Maintenance ................................................................................................................................ 19
Disposal of Waste Materials ...................................................................................................................... 19

MESSAGES AND INFORM ATION

APPENDIX A

Table of Messages .................................................................................................................................... 21
System Information Log ............................................................................................................................ 22
Serial and Part Number Location ............................................................................................................... 22

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Summary of Contents for WAM

Page 1: ...XX XX ENG Rev A1 WIRELESS ACQUISITION MODULE WAM USER MANUAL Manufactured by Mortara Instrument Inc Milwaukee Wisconsin U S A CAUTION Federal law restricts this device to sale by or on the order of a...

Page 2: ...gs to Mortara Instrument Inc No part of this document may be transmitted reproduced used or disclosed outside of the receiving organization without the express written consent of Mortara Instrument In...

Page 3: ......

Page 4: ......

Page 5: ...2 Fax 414 354 4760 E mail techsupport mortara com 24 hour Technical Support Same day Shipment of Replacement Parts Biomedical Training Classes Extended Warranties Service Contracts Sales Support Suppl...

Page 6: ...back of the device Care should be taken so that these numbers are not defaced Copyright and Trademark Notices This document contains information that is protected by copyright All rights are reserved...

Page 7: ...all carrier charges with respect to any Product s returned to Mortara s principal place or any other place as specifically designated by Mortara or an authorized distributor or representative of Mort...

Page 8: ...To maintain designed operator and patient safety peripheral equipment and accessories used that can come in direct patient contact must be in compliance with UL 60601 1 IEC 60601 1 and IEC 60601 2 25...

Page 9: ...the device may be adversely affected by the use of other medical equipment including but not limited to defibrillators and ultrasound machines There is no known safety hazard if other equipment such...

Page 10: ...evice will only work with receiving devices that are equipped with the appropriate option No user serviceable parts are inside Damaged or suspected inoperative equipment must be immediately removed fr...

Page 11: ...or doctor s office setting and should be used and stored according to the environmental conditions specified below Ambient Temperature Range 0 C to 45 C 32 F to 113 F Relative Humidity Range 5 to 95 n...

Page 12: ...Operation is subject to the following conditions 1 This device may not cause harmful interference and 2 This device must accept any interference received including interference that may cause undesir...

Page 13: ...ce is classified as follows Class I equipment or internally powered Type CF ECG defibrillation proof applied parts IPX1 with regards to the harmful ingress of water Equipment not suitable for use in t...

Page 14: ...int On Off button Battery with notification See operating instructions for type of cell to be used Indicates compliance to applicable EEC directives Do not dispose as unsorted municipal waste Per EC D...

Page 15: ...ct buttons and controls for proper function and appearance Cleaning and Disinfection Refer to section 3 for proper cleaning and disinfection procedures Sterilization EtO sterilization is not recommend...

Page 16: ...s between the radio equipment and the device The use of accessories and cables other than those specified below may result in increased emissions or decreased immunity of the device Description Part N...

Page 17: ...xiii BATTERY CAP ASSEMBLY WAM 8356 008 51...

Page 18: ...unity The equipment is intended for use in the electromagnetic environment specified in the table below The customer or the user of the equipment should ensure that it is used in such an environment E...

Page 19: ...recommended separation distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site surveya should be less than the compliance level in each frequency rang...

Page 20: ...Power of Transmitter W Separation Distance According to Frequency of Transmitter m 150 KHz to 800 MHz 800 MHz to 2 5 GHz P d 2 1 P d 3 2 0 01 0 1 m 0 2 m 0 1 0 4 m 0 7 m 1 1 2 m 2 3 m 10 4 0 m 7 0 m 1...

Page 21: ...Cover 7 Battery Installation 7 Attaching the Patient Lead Wires 7 Turning the WAM On 8 Turning the WAM Off 8 Connecting the WAM to the ELI 350 Pairing Mode 8 Patient ECG Hookup 9 Positioning the Elec...

Page 22: ...ON 3 Cleaning the WAM Transmitter and ECG Cable 19 Periodic Maintenance 19 Disposal of Waste Materials 19 MESSAGES AND INFORMATION APPENDIX A Table of Messages 21 System Information Log 22 Serial and...

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