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RapidFor™ Ketamine HCl (KET) Rapid Test Kit (Urine)

EUDAMED

Class IVD General (EU MDR)

Ref VDOA18

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ Ketamine HCl (KET) Rapid Test Kit (Urine) EUDAMED
Device Name
Ketamine HCl (KET) Rapid Test Kit (Urine) EUDAMED
Model / Reference
VDOA18 EUDAMED

Identifiers

Primary DI / UDI-DI
08683548251374 EUDAMED
Basic UDI-DI
B-08683548251374 EUDAMED
EMDN Code
W0102160599 DRUGS OF ABUSE/TOXICOLOGY RT & POC - OTHER 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

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

RapidFor™ Ketamine HCl (KET) Rapid Test Kit (Urine) by Vitrosens Biotechnology Inc. — 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
TR-MF-000026452

Sources (1)

  • EUDAMED 9483f0ea-98c1-47da-9b83-a53d8b26e3c1 61 fields · synced Jul 9, 2026