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AMH Rapid Quantitative Test

EUDAMED

Class IVD General (EU MDR)

Ref BT2213

by Xiamen Biotime Biotechnology Co., Ltd.

Identity

Device Name
AMH Rapid Quantitative Test EUDAMED
Model / Reference
BT2213 EUDAMED

Identifiers

Primary DI / UDI-DI
06933260211777 EUDAMED
Basic UDI-DI
B-06933260211777 EUDAMED
EMDN Code
W0102160999 INDIVIDUAL AND SPECIFIC HORMONES/PROTEINS RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain 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

AMH Rapid Quantitative Test by Xiamen Biotime Biotechnology Co., Ltd. — Class IVD General — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000012852
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 1f6345a9-6770-4c99-9e8e-69c680053d88 61 fields · synced Oct 6, 2026