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Oral Fluid Drug Test Kit (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref FBxxx-702a

by Zhejiang Orient Gene Biotech Co., Ltd

Identity

Trade Name
Oral Fluid Drug Test Kit (FIA) EUDAMED
Device Name
Oral Fluid Drug Test Kit (FIA) EUDAMED
Model / Reference
FBxxx-702a EUDAMED

Identifiers

Primary DI / UDI-DI
D-FBxxx-702aWL EUDAMED
Basic UDI-DI
B-FBxxx-702aWL EUDAMED
EMDN Code
W0102160511 MULTIPLE DRUGS OF ABUSE/TOXICOLOGY RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Oral Fluid Drug Test Kit (FIA) by Zhejiang Orient Gene Biotech 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-000017965
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED ec05d6dc-dbf1-45c4-9c1f-99b8798242d4 61 fields · synced Jul 19, 2026