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RADI Human Papillomavirus Detection Kit
EUDAMEDClass IVD General (EU MDR)
Ref RS002
Identity
- Device Name
- RADI Human Papillomavirus Detection Kit EUDAMED
- Model / Reference
- RS002 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08800204300669 EUDAMED
- Basic UDI-DI
- B-08800204300669 EUDAMED
- EMDN Code
- W0105041099 HPV REAGENTS - OTHER EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
RADI Human Papillomavirus Detection Kit by KH Medical Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-08800204300669 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- KH Medical Co., Ltd.
- EUDAMED SRN
- KR-MF-000017883
- Authorised Representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Sources (1)
- EUDAMED fc1f9055-ef6a-404d-8365-8ef5b7c26325 61 fields · synced Jun 18, 2026