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RapidFor™ Saliva Multi-Drug Test Kit (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref VMPO86Ref VDOA07Ref VDOA01

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ Saliva Multi-Drug Test Kit (FIA) EUDAMED
RapidFor™ Saliva Multi-Drug Test Kit EUDAMED
Device Name
Saliva Multi-Drug Test Kit (FIA) EUDAMED
Saliva Multi-Drug Test Kit EUDAMED
Model / Reference
VMPO86 EUDAMED
VDOA07 EUDAMED
VDOA01 EUDAMED

Identifiers

Primary DI / UDI-DI
08684595030110 EUDAMED
08683548251268 EUDAMED
08683548250971 EUDAMED
Basic UDI-DI
B-08684595030110 EUDAMED
B-08683548251268 EUDAMED
B-08683548250971 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

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

RapidFor™ Saliva Multi-Drug Test Kit (FIA) 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 (3)

  • EUDAMED bf7d843a-8daf-423b-96c4-c06b3d00165b 61 fields · synced Sep 30, 2026
  • EUDAMED 3fc5de08-c9c2-4644-84ab-0f79ed416f35 61 fields · synced May 17, 2026
  • EUDAMED 226d9fb7-8a7a-4075-a718-be3d56d3ae60 61 fields · synced May 18, 2026