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AmoyDx® NRAS Mutation Detection Kit
EUDAMEDClass IVD General (EU MDR)
Ref 8.01.0172Model 24 tests/kitRef 8.01.0028Model 8 tests/kitRef 8.01.0027
Identity
- Device Name
- AmoyDx® NRAS Mutation Detection Kit EUDAMED
- Model / Reference
- 24 tests/kit EUDAMED8.01.0172 EUDAMED8 tests/kit EUDAMED8.01.0028 EUDAMED8.01.0027 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06959094206130 EUDAMED06959094210762 EUDAMED06959094210618 EUDAMED
- Basic UDI-DI
- B-06959094206130 EUDAMEDB-06959094210762 EUDAMEDB-06959094210618 EUDAMED
- EMDN Code
- W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER EUDAMED
Classification
- Device Class
- Class IVD General 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
AmoyDx® NRAS Mutation Detection Kit by Amoy Diagnostics 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-06959094206130 | Class IVD General | 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 (3)
- EUDAMED 4a0105cf-84df-40bd-8516-fa1bd34a233a 61 fields · synced Jul 28, 2026
- EUDAMED 32c566ce-2e27-4287-b91c-46ee1f7d8bb7 61 fields · synced May 17, 2026
- EUDAMED b82c10b1-4c92-4c3f-9794-113dbb6edd7a 61 fields · synced May 17, 2026