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RapidFor™ Rhinovirus + ADV Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref VMD158 Model VMD158SC

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ Rhinovirus + ADV Test Kit EUDAMED
Device Name
Rhinovirus + ADV Test Kit EUDAMED
Model / Reference
VMD158SC EUDAMED
VMD158 EUDAMED

Identifiers

Primary DI / UDI-DI
08684998270014 EUDAMED
Basic UDI-DI
B-08684998270014 EUDAMED
EMDN Code
W0105090699 OTHER MULTIPLE PATHOGENS - 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™ Rhinovirus + ADV 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 (1)

  • EUDAMED dc02fff9-3f6a-417b-ba06-d35711ae2f75 61 fields · synced Jul 22, 2026