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