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If a serious incident occurs in relation to this medical device, affecting the user, or the patient then the user or
Si se produce un incidente grave en relación con este producto sanitario que afecte al usuario o al paciente, el
patient should report the serious incident to the medical device manufacturer or the distributor.
usuario o el paciente deberán notificarlo al fabricante o al distribuidor del producto sanitario.
En la Unión Europea, el usuario también debe notificar el incidente grave a la autoridad competente en el Estado
In the European Union, the user should also report the serious incident to the Competent Authority in the
miembro en el que se encuentra.
member state where they are located.
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 [email protected]
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 2019
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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