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RIDA®Plex STI 16 well Step 1
EUDAMEDClass IVD Annex II List B (EU MDR)
Ref 27112S
Identity
- Trade Name
- RIDA®Plex STI 16 well Step 1 EUDAMED
- Device Name
- RIDA®Plex STI 16 well EUDAMED
- Model / Reference
- 27112S EUDAMED
Identifiers
- Primary DI / UDI-DI
- 09343044006876 EUDAMED
- Basic UDI-DI
- B-09343044006876 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 1 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-09343044006876 | Class IVD Annex II List B | Active |
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Manufacturer
- Manufacturer
- AusDiagnostics Pty Ltd
- EUDAMED SRN
- AU-MF-000020558
- Authorised Representative
- R-Biopharm AG DE-AR-000050025
Sources (1)
- EUDAMED 83023db4-cccb-4cf3-81c4-c0e403e20875 61 fields · synced Jul 9, 2026