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En cas d'incident grave lié à ce dispositif médical, affectant l'utilisateur ou le patient, celui-ci doit
If a serious incident occurs in relation to this medical device, affecting the user, or the patient then the user or
signaler l'incident grave au fabricant du dispositif médical ou au distributeur.
patient should report the serious incident to the medical device manufacturer or the distributor.
Au sein de l'Union européenne, l'utilisateur doit également signaler l'incident grave à l'autorité
In the European Union, the user should also report the serious incident to the Competent Authority in the
member state where they are located.
compétente de l'État membre où il se trouve.
Manufactured in the UK by Huntleigh Healthcare Ltd on behalf of;
ArjoHuntleigh AB
Hans Michelsensgatan 10
211 20 Malmö, Sweden
Huntleigh Healthcare Ltd.
35 Portmanmoor Road, Cardiff, CF24 5HN, United Kingdom
T: +44 (0)29 20485885 sales@huntleigh-diagnostics.co.uk
www.huntleigh-diagnostics.com
Registered No: 942245 England & Wales. Registered Office:
ArjoHuntleigh House, Houghton Hall Business Park, Houghton Regis, Bedfordshire, LU5 5XF
©Huntleigh Healthcare Limited 2016
A Member of the Arjo Family
and
are trademarks of Huntleigh Technology Limited
As our policy is one of continuous improvement, we reserve the right to modify designs without prior notice.
AW:: 1001048-2
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