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Mortara WAM Скачать руководство пользователя страница 22

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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Содержание WAM

Страница 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...

Страница 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...

Страница 3: ......

Страница 4: ......

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

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

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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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