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RIDASCREEN® Stop

EUDAMED

Class A (EU MDR)

Ref 3080V00-VK

by R-Biopharm AG

Identity

Device Name
RIDASCREEN® Stop EUDAMED
Model / Reference
3080V00-VK EUDAMED

Identifiers

Primary DI / UDI-DI
04049095000034 EUDAMED
Basic UDI-DI
40490953080V00VK0UR EUDAMED
EMDN Code
W0105900201 BUFFERS (UNASSIGNABLE ), SUPPLEM. REAGENTS, ETC EUDAMED

Classification

Device Class
Class A 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

RIDASCREEN® Stop by R-Biopharm AG — Class A — 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 a363c1fc-75a5-4342-8999-ee39d9288143 61 fields · synced Oct 6, 2026