Joe,
 
You may find all your answers TOMORROW if you attend the IVDD seminar at TUV
Rheinland of North America,,Pleasanton, CA  office.
 
If you are unable to make it to the seminar, please contact:
 
 
TUV Rheinland of North America, Inc.
Medical Division
Dr. Stephanie Horn
Program Manager, IVDD

TEL (925) 249 9123 Ext. 131
FAX (925) 249 9124
Email: [email protected]
Address: 1279 Quarry Lane, Pleasanton, CA 94566
www.tuv.com
 
 

 

http://www.us.tuv.com/training_and_educ
tion/seminars2003/2003-04-15_europian_union_pleasanton.html



Joe P Martin <[email protected]> wrote:


Greetings,

The In-Vitro Diagnostics Directive requires that any manufacturer who
places a device on the market notify the competent authorities of the
Member State(s) in which he has his registered place of business. I have a
couple of questions in regards to this requirement.

1. Does this mean that we have to register with every regulatory
authority in all Member States, or is registration with one Member State
sufficient? The product is not manufactured in the EU, yet we do have
places of business in several Member States.

2. For General IVD devices, how does a U.S. manufacturer register their
product in Europe?

3. Does anyone have a list of the regulatory authorities for all Member
States?

As always, your responses are greatly appreciated.

Regards

Joe Martin
Applied Biosystems
martinjp@appliedbiosystems.! com





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