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RIDA®Plex Vaginitis and Vaginosis 12 well Step 1

EUDAMED

Class IVD General (EU MDR)

Ref 87124S

by AusDiagnostics Pty Ltd

Identity

Trade Name
RIDA®Plex Vaginitis and Vaginosis 12 well Step 1 EUDAMED
Device Name
RIDA®Plex Vaginitis and Vaginosis 12 well EUDAMED
Model / Reference
87124S EUDAMED

Identifiers

Primary DI / UDI-DI
09343044006975 EUDAMED
Basic UDI-DI
B-09343044006975 EUDAMED
EMDN Code
W0105070203 GRAM+ - GRAM- - FUNGI - MULTIPLEX ASSAYS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

RIDA®Plex Vaginitis and Vaginosis 12 well Step 1 by AusDiagnostics Pty Ltd — 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

EUDAMED SRN
AU-MF-000020558
Authorised Representative
R-Biopharm AG DE-AR-000050025

Sources (1)

  • EUDAMED 78e98b48-e994-4bb2-98bc-d84bb8ecc5da 61 fields · synced Jul 11, 2026