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Amphetamine (AMP) Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref P22038

by Beijing Jinwofu Bioengineering Technology Co., Ltd.

Identity

Trade Name
Amphetamine (AMP) Rapid Test EUDAMED
Device Name
Amphetamine (AMP) Rapid Test EUDAMED
Model / Reference
P22038 EUDAMED

Identifiers

Primary DI / UDI-DI
06974854620889 EUDAMED
Basic UDI-DI
B-06974854620889 EUDAMED
EMDN Code
W0102090102 AMPHETAMINE/METHAMPHETAMINE SPECIFIC 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

Amphetamine (AMP) Rapid Test by Beijing Jinwofu Bioengineering Technology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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 b373665e-ab9a-4b20-892f-239b84c7ec3a 61 fields · synced Jun 18, 2026