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Ridascreen® Tb

EUDAMED

Class C (EU MDR)

Ref TC8806

by R-Biopharm AG

Identity

Device Name
RIDASCREEN® TB EUDAMED
Model / Reference
TC8806 EUDAMED

Identifiers

Primary DI / UDI-DI
04049095200052 EUDAMED
Basic UDI-DI
4049095TC88060000MU EUDAMED
EMDN Code
W0105010799 MYCOBACTERIA REAGENTS - OTHER EUDAMED

Classification

Device Class
Class C 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® Tb by R-Biopharm AG — Class C — 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 a5c0dba3-661c-4128-aa71-a1b3006cde84 61 fields · synced Oct 7, 2026