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RIDA®GENE Legionella

EUDAMED

Class IVD General (EU MDR)

Ref PG8005

by R-Biopharm AG

Identity

Device Name
RIDA®GENE Legionella EUDAMED
Model / Reference
PG8005 EUDAMED

Identifiers

Primary DI / UDI-DI
04049095160400 EUDAMED
Basic UDI-DI
B-04049095160400 EUDAMED
EMDN Code
W0105010503 LEGIONELLA DETECTION BY NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General 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

RIDA®GENE Legionella by R-Biopharm AG — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

Manufacturer
R-Biopharm AG
EUDAMED SRN
DE-MF-000007993

Sources (1)

  • EUDAMED 33a3af96-9213-48c7-bef1-cec018f587b4 61 fields · synced Jul 20, 2026