Identity
- Device Name
- AmoyDx® FFPE RNA Kit EUDAMED
- Model / Reference
- 36 tests/kit EUDAMED8.02.0003 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06959094210465 EUDAMED
- Basic UDI-DI
- 69590942A0009GJ EUDAMED
- EMDN Code
- W050299 DEVICES FOR SAMPLES TRANSPORT - OTHER EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Northern Ireland 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
New Device
No
EUDAMED
AmoyDx® FFPE RNA Kit by Amoy Diagnostics Co., LTD. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 69590942A0009GJ | Class A | Active |
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Manufacturer
- Manufacturer
- Amoy Diagnostics Co., LTD.
- EUDAMED SRN
- CN-MF-000021843
- Authorised Representative
- QbD RepS BV BE-AR-000000040
Sources (1)
- EUDAMED 66fbe019-5e9b-4932-918d-26f6111f2a47 61 fields · synced Jun 19, 2026