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AMH Quantitative Test Kit (Time-Resolved FIA)

EUDAMED

Class IVD General (EU MDR)

Ref FAAMH-302a

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-302a EUDAMED

Identifiers

Primary DI / UDI-DI
D-FAAMH-302aRG EUDAMED
Basic UDI-DI
B-FAAMH-302aRG 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

Yes

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 0b491466-228d-42ef-90bd-ece384e632dc 61 fields · synced Jun 19, 2026