← Back to catalogue

Buprenorphine (BUP) Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref P22041

by Beijing Jinwofu Bioengineering Technology Co., Ltd.

Identity

Trade Name
Buprenorphine (BUP) Rapid Test EUDAMED
Device Name
Buprenorphine (BUP) Rapid Test EUDAMED
Model / Reference
P22041 EUDAMED

Identifiers

Primary DI / UDI-DI
06974854620919 EUDAMED
Basic UDI-DI
B-06974854620919 EUDAMED
EMDN Code
W0102090117 BUPRENORPHINE 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

Buprenorphine (BUP) 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000035739
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED be9ae5c6-7254-423b-8cd0-1ec40f3c0b70 61 fields · synced Jul 9, 2026