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Huntleigh Sonicaid Team 3 Series - Page 5

Huntleigh Sonicaid Team 3 Series
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5
Table of Contents
17. Speci cations .................................................................. 93
17.1 Equipment Classi cation .....................................................................93
17.2 General ...................................................................................................93
17.3 Environmental ........................................................................................93
17.4 Transducers .......................................................................................... 94
17.5 Printer .................................................................................................... 97
17.6 Connections * ......................................................................................... 98
17.7 Display ................................................................................................... 99
17.8 Default Settings ....................................................................................99
17.9 General Standards .................................................................................101
18. Accessories ..................................................................... 102
19. Electromagnetic Compatibility ........................................ 103
20. Ultrasound Safety Considerations ................................... 107
21. End of Life Disposal .......................................................... 110
22. Warranty & Service .......................................................... 111
© Huntleigh Healthcare Ltd
All rights reserved
Manufactured in the UK by Huntleigh Healthcare Ltd.
As part of the ongoing development programme the company reserves the right
to modify speci cations and materials without notice.
Sonicaid and Huntleigh are registered trademarks of Huntleigh Technology Ltd.
2016.
© Huntleigh Healthcare Ltd. 2016
Team 3 is in conformity with the Medical Devices Directive 93/42/EEC
as amended by 2007/47/EC and has been subject to the conformity
assurance procedures laid down by the Council Directive

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