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Rida®seek

EUDAMED

Class A (EU MDR)

Ref ZRIDASEEK

by R-Biopharm AG

Identity

Device Name
RIDA®SEEK EUDAMED
Model / Reference
ZRIDASEEK EUDAMED

Identifiers

Primary DI / UDI-DI
04049095260674 EUDAMED
Basic UDI-DI
4049095ZRIDASEEK0FN EUDAMED
EMDN Code
W02050182 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class A EUDAMED
Special Device Type
Software 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

No

EUDAMED

New Device

No

EUDAMED

Rida®seek 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 074f2137-8b63-49ab-b91b-3a3ec580df74 61 fields · synced Sep 18, 2026