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AMH Rapid Quantitative Test

EUDAMED

Class IVD General (EU MDR)

Ref 2942Model 25 servings/box

by Coei Biotech Co.Ltd.

Identity

Trade Name
AMH Rapid Quantitative Test EUDAMED
Device Name
AMH Rapid Quantitative Test EUDAMED
Model / Reference
25 servings/box EUDAMED
2942 EUDAMED

Identifiers

Primary DI / UDI-DI
06977565582941 EUDAMED
Basic UDI-DI
B-06977565582941 EUDAMED
EMDN Code
W0102050215 ANTI-MULLERIAN HORMONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

AMH Rapid Quantitative Test by Coei Biotech 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-000049509
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 79116849-93b8-45d0-8c0c-e7ec178b21b9 61 fields · synced Jun 18, 2026