Serum Amyloid A Chemiluminescence Immunoassay Kit

EUDAMED

Class IVD General (EU MDR)

Ref S2151E-50

by Sansure Biotech Inc.

Identity

Device Name: Serum Amyloid A Chemiluminescence Immunoassay Kit EUDAMED
Model / Reference: S2151E-50 EUDAMED

Identifiers

Primary DI / UDI-DI: 06955792742857 EUDAMED
Basic UDI-DI: B-06955792742857 EUDAMED
EMDN Code: W0102019013 BETA-AMYLOID (1-40) EUDAMED

Classification

Device Class: Class IVD General EUDAMED
Market of Registration: France EUDAMED

Clinical & Handling

Sterile

EUDAMED

Human Tissues

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

EUDAMED

Near-Patient Testing

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

EUDAMED

Surgical Instrument

EUDAMED

Serum Amyloid A Chemiluminescence Immunoassay Kit by Sansure Biotech Inc. — 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

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	CE/IVDD	B-06955792742857	Class IVD General	Active

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Manufacturer

Manufacturer: Sansure Biotech Inc.
EUDAMED SRN: CN-MF-000011392
Authorised Representative: Obelis s.a. BE-AR-000000106

Sources (1)

EUDAMED ac3756a4-b04e-4413-aec7-17701aeea4c3 61 fields · synced Jun 17, 2026