Mortara WAM User Manual
  1. Manuals
  2. Brands
  3. Mortara Manuals
  4. Control Unit
  5. WAM
  6. User manual

Mortara WAM User Manual

Wireless acquisition module
Hide thumbs

Advertisement

Table of Contents

Ref 9515-XXX-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 physician.

Advertisement

Table of Contents
loading
Need help?

Need help?

Do you have a question about the WAM and is the answer not in the manual?

Questions and answers

Summary of Contents for Mortara WAM

  • Page 1 Ref 9515-XXX-XX-ENG Rev A1 WIRELESS ACQUISITION MODULE 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 physician.
  • Page 2 7865 N. 86th Street Milwaukee, Wisconsin 53224 This document contains confidential information that belongs 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, Inc. Mortara is a registered trademark of Mortara Instrument,...

  • Page 5: Technical Support And Service

    414.354.4760 Internet: http://www.mortara.com E-mail: sales@mortara.com European Union Representative Mortara Instrument Germany Kaninenberghöhe 50 45136 Essen Mortara Rangoni Europe, Srl Germany (European Headquarters) Tel: +49.201.18 55 69 70 Via Cimarosa 103/105 Fax: +49.201.18 55 69 77 40033 Casalecchio di Reno (BO)
  • Page 6 Failure to do so may cause undue failure and possible health hazards. Equipment Identification Mortara Instrument, Inc. equipment is identified by a serial and reference number on the back of the device. Care should be taken so that these numbers are not defaced.

  • Page 7: Warranty Information

    Mortara or an authorized distributor or representative of Mortara, and (ii) all risk of loss in transit. It is expressly agreed that the liability of Mortara is limited and that Mortara does not function as an insurer. A...

  • Page 8: User Safety Information

    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. Only use parts and accessories supplied with the device and available through Mortara Instrument, Inc. ·...
  • Page 9 other adverse reactions. Electrodes are intended for short term use and should be removed from the patient promptly following testing. · FCC Warning (Part 15.21): Changes or modifications not expressly approved by the party responsible for compliance could void the user s authority to operate the device. ·...
  • Page 10 Caution(s) · To prevent possible damage to the device, do not use sharp or hard objects to depress buttons, only use fingertips. · Do not attempt to clean the device or patient cables by submersing into a liquid, autoclaving, or steam cleaning as this may damage equipment or reduce its usable life.
  • Page 11 · This device is intended to be used in a hospital 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% (non-condensing) Atmosphere Pressure: 500 hPa to 1060 hPa...

  • Page 12: Fcc Compliance Statement

    FCC Warning (Part 15.21): Changes or modifications not expressly approved by the party responsible for compliance could void the user s authority to operate the device. WAM FCC ID: HJR-WAM2500 These devices comply with Part 15 of the FCC rules. Operation is subject to the following conditions: 1.
  • Page 13 Note(s) · Proper patient preparation is important to proper application of ECG electrodes and operation of the device. · If an electrode is not properly connected to the patient, or one or more of the patient cable lead wires is damaged, display will indicate a lead fault for the lead(s) where the condition is present.

  • Page 14: Equipment Symbols

    Equipment Symbols Symbol Delineation Attention, consult accompanying documents Defibrillator-proof, type CF applied part Acquire 12 Lead ECG Acquire Rhythm Print 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.
  • Page 15 General Care Precautions · Turn off the device before inspecting or cleaning. · Do not immerse the device in water. · Do not use organic solvents, ammonia-based solutions, or abrasive cleaning agents which may damage equipment surfaces. Inspection Inspect your equipment daily prior to operation. If you notice anything that requires repair, contact an authorized service person to make the repairs.

  • Page 16: Electromagnetic Compatibility (Emc)

    The use of accessories and cables other than those specified below, may result in increased emissions or decreased immunity of the device. Description Part Number LEAD SET WAM 10 WIRE BANANA AHA 9293-046-50 LEAD SET WAM 10 WIRE BANANA IEC 9293-046-51...
  • Page 17 BATTERY CAP ASSEMBLY WAM 8356-008-51 xiii...
  • Page 18 Table X-1 Guidance and Manufacturer s Declaration: Electromagnetic Emissions 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. Emissions Test Compliance Electromagnetic Environment: Guidance...
  • Page 19 Table X-3 Guidance and Manufacturer s Declaration: Electromagnetic Immunity 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. Emissions Test IEC 60601 Compliance...
  • Page 20 Table X-4 Recommended Separation Distances Between Portable and Mobile RF Communications Equipment and the Equipment The equipment is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the equipment can help to prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the equipment as recommended in the table below, according to the maximum output power of the communications equipment.
  • Page 21 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 Electrodes for 10-wire Hookup ................... 9 LED Display Battery Voltage Indicator .......................

  • Page 22: Maintenance Section

    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...

Table of Contents

Save PDF