AIMDD – Active Implantable Medical Devices Directive

The Active Medical Device Directive (AIMDD)  gives manufacturers the opportunity to develop their own compliance program. We guide you through the entire process and assist to optimize your compliance program to meet your product specifications and business needs.

AIMDD

1 Appoint your European Authorized Representative
Ask for our quotation!
2 Identify all EU Directives applicable to your product (such as AIMDD, WEEE, EMC, etc.) We will assist!
3 Identify the applicable harmonized standards for your product We will provide a list!
4 Check your device against the Essential Requirements (Annex I) We will provide a checklist!
5 Select and perform the Conformity Assessment Procedure applicable to your product We will guide you through!
6 Prepare a Technical File and (if applicable) implement a Quality Management System We will assist!
7 Select a Notified Body (if applicable) and sign your Declaration of Conformity We will provide lists and forms!


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Düsseldorf / Germany – 20-23 November 2013

 

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