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AMH Quantitative Test Kit (Time-Resolved FIA)

EUDAMED

Class IVD General (EU MDR)

Ref FAAMH-402a

by Zhejiang Orient Gene Biotech Co., Ltd

Identity

Trade Name
AMH Quantitative Test Kit (Time-Resolved FIA) EUDAMED
Device Name
AMH Quantitative Test Kit (Time-Resolved FIA) EUDAMED
Model / Reference
FAAMH-402a EUDAMED

Identifiers

Primary DI / UDI-DI
D-FAAMH-402aRP EUDAMED
Basic UDI-DI
B-FAAMH-402aRP EUDAMED
EMDN Code
W0102050215 ANTI-MULLERIAN HORMONE 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

AMH Quantitative Test Kit (Time-Resolved FIA) by Zhejiang Orient Gene Biotech Co., Ltd — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000017965
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED fa05e261-db12-415d-aa97-18faf2ee514f 61 fields · synced Jul 8, 2026