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Rida®q3

EUDAMED

Class A (EU MDR)

Ref ZRQ3

by R-Biopharm AG

Identity

Device Name
RIDA®Q3 EUDAMED
Model / Reference
ZRQ3 EUDAMED

Identifiers

Primary DI / UDI-DI
04049095260155 EUDAMED
Basic UDI-DI
4049095ZRQ3000000FP EUDAMED
EMDN Code
W0201020201 IMMUNOCHEMISTRY READERS 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

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Rida®q3 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 7e4d91b6-845a-464d-9714-0cc4d582a4a7 61 fields · synced Jun 18, 2026