Dear Members,

In the EEC if I register a Class I Medical Device with a Competent Authority
in one Membered State, must I register with other Competent Authorities as
we eventually market product their State. All input is appreciated.

Regards,

Mark Schmidt
X-Rite Incorporated
Grandville, MI  
U.S.A.

[email protected]
phone - 616 257 2469





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