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AmoyDx® KRAS/NRAS/BRAF Mutations Detection Kit

EUDAMED

Class IVD General (EU MDR)

Ref 8.01.0033Model 6 tests/kitRef 8.01.0034

by Amoy Diagnostics Co., LTD.

Identity

Device Name
AmoyDx® KRAS/NRAS/BRAF Mutations Detection Kit EUDAMED
Model / Reference
6 tests/kit EUDAMED
8.01.0033 EUDAMED
8.01.0034 EUDAMED

Identifiers

Primary DI / UDI-DI
06959094210649 EUDAMED
06959094210922 EUDAMED
Basic UDI-DI
B-06959094210649 EUDAMED
B-06959094210922 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® KRAS/NRAS/BRAF Mutations 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

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Manufacturer

EUDAMED SRN
CN-MF-000021843
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (2)

  • EUDAMED 3eb7cd97-d273-4c43-9f87-f6a053fc559c 61 fields · synced Jul 29, 2026
  • EUDAMED e24d7136-7626-4c33-9d2b-1fdbd8ecdc1d 61 fields · synced May 17, 2026