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RIDASCREEN® Control -

EUDAMED

Class A (EU MDR)

Ref 3056C00-VK

by R-Biopharm AG

Identity

Device Name
RIDASCREEN® Control - EUDAMED
Model / Reference
3056C00-VK EUDAMED

Identifiers

Primary DI / UDI-DI
04049095000041 EUDAMED
Basic UDI-DI
40490953056C00VK0NF 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

Yes

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® Control - 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 679f232b-5df4-4267-aa1f-9fdbce4ac999 61 fields · synced Oct 6, 2026