Si se produce un incidente grave en relación con este producto sanitario que afecte al usuario o al
If a serious incident occurs in relation to this medical device, affecting the user, or the patient then the user or
patient should report the serious incident to the medical device manufacturer or the distributor.
paciente, el usuario o el paciente deberán notificarlo al fabricante o al distribuidor del producto sanitario.
In the European Union, the user should also report the serious incident to the Competent Authority in the
En la Unión Europea, el usuario también debe notificar el incidente grave a la autoridad competente en
member state where they are located.
el Estado miembro en el que se encuentra.
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 2011
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.
1001048-3
www.huntleigh-diagnostics.com/
www.huntleigh-healthcare.us/
