← Back to catalogue
RIDA®Plex Vaginitis and Vaginosis 8 well Step 2
EUDAMEDClass IVD General (EU MDR)
Ref 27117P
Identity
- Trade Name
- RIDA®Plex Vaginitis and Vaginosis 8 well Step 2 EUDAMED
- Device Name
- RIDA®Plex Vaginitis and Vaginosis 8 well EUDAMED
- Model / Reference
- 27117P EUDAMED
Identifiers
- Primary DI / UDI-DI
- 09343044006906 EUDAMED
- Basic UDI-DI
- B-09343044006906 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 8 well Step 2 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-09343044006906 | Class IVD General | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- AusDiagnostics Pty Ltd
- EUDAMED SRN
- AU-MF-000020558
- Authorised Representative
- R-Biopharm AG DE-AR-000050025
Sources (1)
- EUDAMED f82ab854-a07c-4adb-91f7-592163f771a3 61 fields · synced Jul 24, 2026