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EDDP Rapid Test i

EUDAMED

Class IVD General (EU MDR)

Ref P22053

by Beijing Jinwofu Bioengineering Technology Co., Ltd.

Identity

Trade Name
EDDP Rapid Test i EUDAMED
Device Name
EDDP Rapid Test EUDAMED
Model / Reference
P22053 EUDAMED

Identifiers

Primary DI / UDI-DI
06974854621039 EUDAMED
Basic UDI-DI
B-06974854621039 EUDAMED
EMDN Code
W0102090110 METHADONE 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

EDDP Rapid Test i 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 fdfb6814-89af-4e3f-8b98-bf51dd0ea5ce 61 fields · synced Jun 18, 2026