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Brucella Antibody Rapid Test Kit (Lateral Flow Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref 0201002853Model 10 tests/kit

by Beijing Kinghawk Pharmaceutical CO., Ltd

Identity

Trade Name
Brucella Antibody Rapid Test Kit (Lateral Flow Immunoassay) EUDAMED
Device Name
Brucella Antibody Rapid Test Kit (Lateral Flow Immunoassay) EUDAMED
Model / Reference
10 tests/kit EUDAMED
0201002853 EUDAMED

Identifiers

Primary DI / UDI-DI
06971140521226 EUDAMED
Basic UDI-DI
B-06971140521226 EUDAMED
EMDN Code
W01050499 VIROLOGY REAGENTS - 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

Brucella Antibody Rapid Test Kit (Lateral Flow Immunoassay) by Beijing Kinghawk Pharmaceutical 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-000052726
Authorised Representative
Medunion S.L. ES-AR-000019366

Sources (1)

  • EUDAMED 4252981c-f9ea-4c28-97aa-66831f6f3e7c 61 fields · synced Jun 18, 2026