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Virgin Island (UK)

Product:
In-Vitro Diagnostic Medical Devices Regulation

1. Application form

-Full name, address, email, phone

-An authorization letter if acting on behalf of a company

2. Apply online

3. No need LR

4. Technical document 

-Test reports from accredited labs certifying compliance with EMC, RF, and electrical safety standards.

-Equipment Type Approval Certificate from a reputable approving body (FCC, ETSI, etc.)

-Original Type Approval Certificate

-Technical specifications: frequency range, power, modulations

-User  manual, block diagrams

5. Accept FCC, CE

6. Equipment detail 

-Product description, specific application

-Manufacturer, brand, model, serial, type, class, category
-Manufacturing country
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