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Serum Amyloid A(SAA)Assay Kit

EUDAMED

Class IVD General (EU MDR)

Ref 69543760F000756QModel 100 Tests

by Beijing Leadman Biochemistry Co., Ltd.

Identity

Trade Name
Serum Amyloid A(SAA)Assay Kit EUDAMED
Device Name
Serum Amyloid A(SAA)Assay Kit EUDAMED
Model / Reference
100 Tests EUDAMED
69543760F000756Q EUDAMED

Identifiers

Primary DI / UDI-DI
06954376005579 EUDAMED
Basic UDI-DI
B-06954376005579 EUDAMED
EMDN Code
W01021199 RHEUMATOID / INFLAMMATORY DISEASE MARKERS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

Serum Amyloid A(SAA)Assay Kit by Beijing Leadman Biochemistry 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-000020150
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 708650e1-e12f-412f-905d-cc9090a4ffef 61 fields · synced Jun 18, 2026