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RIDA®Plex STI 16 well Step 2

EUDAMED

Class IVD Annex II List B (EU MDR)

Ref 27112P

by AusDiagnostics Pty Ltd

Identity

Trade Name
RIDA®Plex STI 16 well Step 2 EUDAMED
Device Name
RIDA®Plex STI 16 well EUDAMED
Model / Reference
27112P EUDAMED

Identifiers

Primary DI / UDI-DI
09343044006869 EUDAMED
Basic UDI-DI
B-09343044006869 EUDAMED
EMDN Code
W0105070501 STIS / STDS (C.TRACHOMATIS, N.GONORRHOEAE ,M.GENITALIUM, T.VAGINALIS, UREAPLASMA SPP….) COMBINATION - MULTIPLEX NA REAGENTS EUDAMED

Classification

Device Class
Class IVD Annex II List B 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 STI 16 well Step 2 by AusDiagnostics Pty Ltd — Class IVD Annex II List B — 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 7f941ba5-b7e0-48d6-ab5b-0c47b78ae6ea 61 fields · synced Sep 18, 2026