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Saint Pierre and Miquelon (DOM)

Product:
In-Vitro Diagnostic Medical Devices Regulation

1. Application form

-Full name, address, email, phone, manufacturer

-Payment

-Proof of authorization in favor of their local representative in Burkina Faso

2. Apply online

3. No need LR, only UE Agent

4. Technical document 

-Test reports of conformity issued by accredited laboratories (RF, EMC, Safety)

-Declaration of Conformity

-User manual, design schematics and diagrams

-Technical specification: frequency bands, modulations

-Frequency specification: Technical details of supported frequency bands

-Photographs

5. Accept CE

6. Equipment detail 

-Name, brand, model, manufacturer

-Country of origin
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