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RapidFor™ Rota/Adeno (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref VMPO129Model VMPO129GADModel VMPO129GD

by Vitrosens Biotechnology Inc.

Identity

Trade Name
RapidFor™ Rota/Adeno (FIA) EUDAMED
Device Name
Rota/Adeno (FIA) EUDAMED
Model / Reference
VMPO129GAD EUDAMED
VMPO129 EUDAMED
VMPO129GD EUDAMED

Identifiers

Primary DI / UDI-DI
08684998277693 EUDAMED
08684998271912 EUDAMED
Basic UDI-DI
B-08684998277693 EUDAMED
B-08684998271912 EUDAMED
EMDN Code
W0105040601,W0105040606 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

No

EUDAMEDEUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

RapidFor™ Rota/Adeno (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 (2)

  • EUDAMED eb4b0ab1-2550-46d1-8519-8b86e67933b1 61 fields · synced Oct 6, 2026
  • EUDAMED 3441381c-cfa4-4d9a-95f0-81ab5dc00c65 61 fields · synced May 19, 2026