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Luteinising Hormone (LH) Rapid Test Kit (Immunochromatographic Assay)

EUDAMED

Class IVD General (EU MDR)

Ref ICA2230Model 20 tests/kit

by BioTeke Corporation(Wuxi)Co., Ltd

Identity

Device Name
Luteinising Hormone (LH) Rapid Test Kit (Immunochromatographic Assay) EUDAMED
Model / Reference
20 tests/kit EUDAMED
ICA2230 EUDAMED

Identifiers

Primary DI / UDI-DI
06974541565486 EUDAMED
Basic UDI-DI
B-06974541565486 EUDAMED
EMDN Code
W0102160304 LH - RT & POC 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

Luteinising Hormone (LH) Rapid Test Kit (Immunochromatographic Assay) by Bioteke Corporation (Wuxi) 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-000007517
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED b3770d2b-59da-4ef8-a779-1fa0e0bc6833 61 fields · synced Jul 11, 2026