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RIDASCREEN® Norovirus 3rd Generation

EUDAMED

Class B (EU MDR)

Ref C1401C01-VK

by R-Biopharm AG

Identity

Device Name
RIDASCREEN® Norovirus 3rd Generation EUDAMED
Model / Reference
C1401C01-VK EUDAMED

Identifiers

Primary DI / UDI-DI
04049095030697 EUDAMED
Basic UDI-DI
4049095C140100000HU EUDAMED
EMDN Code
W0105040616 NOROVIRUS EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

RIDASCREEN® Norovirus 3rd Generation by R-Biopharm AG — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
R-Biopharm AG
EUDAMED SRN
DE-MF-000007993

Sources (1)

  • EUDAMED 83bce46f-fbe9-4cee-8772-f3083afce41e 61 fields · synced May 23, 2026