Gima i-PAD CU-SP1 Bruksanvisning
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Inte kategoriserad
i-PAD CU-SP1
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Instructions for Use
i-PAD -SP1 CU
The information in these Instructions for Use applies to the i-PAD CU-SP1. This information is
subject to change. Please contact CU Medical Systems, Inc. or its authorized representatives
for information on revisions.
Revision History
Edition 4
Publication Date: September 28, 2017
Document No.: SP1-OPM-E-04
Published by: CU Medical Systems, Inc.
Printed in the Republic of Korea
Copyright
© 2017 CU Medical Systems, Inc.
No part of these Instructions for Use may be reproduced without the permission of CU Medical
Systems, Inc.
Medical Device Directive
The i-PAD CU-SP1 complies with the requirements of the Medical Device Directive 2007 7/EC /4
and its revisions.
Important:
Quick debrillation is needed if sudden cardiac arrest occurs. Since the chance of success is
reduced by 7% to 10% for every minute that debrillation is delayed, defibrillation must be
performed promptly.
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The i-PAD CU-SP1 is manufactured by:
CU Medical Systems, Inc.
130-1 Donghwagongdan- , Munmak-eup, Wonju-si, ro
Gangwon-do, Republic of Korea
Authorized EU Representative
Medical Device Safety Service
Schigraben 41, 30175 Hannover, Germany
Contact Us
Product and Order Inquiries
Overseas Sales Team
CU Medical Systems, Inc.
5F, Cheonggye Plaza 221, Anyangpangyo-ro, ,
Uiwang-si, Gyeonggi-do, Republic of Korea
Tel : +82 31 421 9700 / Fax: +82 31 421 9911
E-mail addresses : sales@cu911.com
German Branch Oce
CU Medical Germany GmbH, Cicero Str.26,
10709 Berlin, Germany
Tel: +49 30 6781 7804
Fax: +49 30 6782 0901
Service and Technical Support
Customer Service Team
CU Medical Systems, Inc.
5F, Cheonggye Plaza 221, Anyangpangyo-ro, ,
Uiwang-si, Gyeonggi-do, Republic of Korea
Tel : +82 31 421 9700 / Fax: +82 31 421 9911
E-mail addresses : service@cu911.com
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Produktspecifikationer
| Varumärke: | Gima |
| Kategori: | Inte kategoriserad |
| Modell: | i-PAD CU-SP1 |
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