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RapidFor™ Urine Rapid Drug Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref VDOA05

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ Urine Rapid Drug Test Kit EUDAMED
Device Name
Urine Rapid Drug Test Kit EUDAMED
Model / Reference
VDOA05 EUDAMED

Identifiers

Primary DI / UDI-DI
08683548251039 EUDAMED
08683548251022 EUDAMED
Basic UDI-DI
B-08683548251039 EUDAMED
B-08683548251022 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

EUDAMEDEUDAMED

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

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

RapidFor™ Urine Rapid Drug Test Kit by Vitrosens Biotechnology Inc. — 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
TR-MF-000026452

Sources (2)

  • EUDAMED 64349125-05b3-4cd6-936e-cf7e1b566f6e 61 fields · synced Oct 6, 2026
  • EUDAMED 97108012-8c13-4378-ab4f-d59ba74bf8fe 61 fields · synced May 19, 2026