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Serum Amyloid A (SAA) Test

EUDAMED

Class IVD General (EU MDR)

Ref P2206325

by Beijing Jinwofu Bioengineering Technology Co., Ltd.

Identity

Trade Name
Serum Amyloid A (SAA) Test EUDAMED
Device Name
Serum Amyloid A (SAA) Test EUDAMED
Model / Reference
P2206325 EUDAMED

Identifiers

Primary DI / UDI-DI
06974854621138 EUDAMED
Basic UDI-DI
B-06974854621138 EUDAMED
EMDN Code
W0102019099 SPECIFIC PROTEINS - 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

Serum Amyloid A (SAA) Test by Beijing Jinwofu Bioengineering Technology 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-000035739
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 7d559245-a2bb-4f6e-a677-a1ad82390983 61 fields · synced Jun 18, 2026