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Follicle-stimulating Hormone (FSH) Rapid Test Kit (Immunochromatographic Assay)

EUDAMED

Class IVD General (EU MDR)

Ref ICA2229Model 1 test/kit

by BioTeke Corporation(Wuxi)Co., Ltd

Identity

Device Name
Follicle-stimulating Hormone (FSH) Rapid Test Kit (Immunochromatographic Assay) EUDAMED
Model / Reference
1 test/kit EUDAMED
ICA2229 EUDAMED

Identifiers

Primary DI / UDI-DI
06974541565417 EUDAMED
Basic UDI-DI
B-06974541565417 EUDAMED
EMDN Code
W0102050105 LUTEINISING HORMONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Follicle-stimulating Hormone (FSH) Rapid Test Kit (Immunochromatographic Assay) by Bioteke Corporation (Wuxi) Co., Ltd. — Class IVD General — IVDD — listed in…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000007517
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 900c38c5-bd74-43b9-a4a1-66884cf16c12 61 fields · synced Jul 20, 2026