Identity
- Trade Name
- Amplidiag COVID-19 Kit EUDAMED
- Device Name
- Amplidiag COVID-19 Kit EUDAMED
- Model / Reference
- AD-CV-864 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06430041761365 EUDAMED
- Basic UDI-DI
- B-06430041761365 EUDAMED
- EMDN Code
- W0105070503 RESPIRATORY TRACT INFECTIONS - MULTIPLEX NA REAGENTS EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Finland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
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
Amplidiag COVID-19 Kit by Mobidiag Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union No Longer Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-06430041761365 | Class IVD General | No Longer Active |
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Manufacturer
- Manufacturer
- Mobidiag Ltd.
- EUDAMED SRN
- FI-MF-000001215
Sources (1)
- EUDAMED 902f0e8e-5762-4124-94c3-4ee267fb03d7 61 fields · synced Jul 29, 2026