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H-FABP Test

EUDAMED

Class IVD General (EU MDR)

Ref P2207125

by Beijing Jinwofu Bioengineering Technology Co., Ltd.

Identity

Trade Name
H-FABP Test EUDAMED
Device Name
H-FABP Test EUDAMED
Model / Reference
P2207125 EUDAMED

Identifiers

Primary DI / UDI-DI
06974854621237 EUDAMED
Basic UDI-DI
B-06974854621237 EUDAMED
EMDN Code
W01021302 HEART-TYPE FATTY ACID BINDING PROTEIN 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

H-FABP 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 03c235fd-44ae-4bab-8e9b-0a746e93f67c 61 fields · synced Jun 17, 2026