Identity
- Device Name
- RIDA®GENE Bordetella EUDAMED
- Model / Reference
- PG2505 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04049095160325 EUDAMED
- Basic UDI-DI
- B-04049095160325 EUDAMED
- EMDN Code
- W0105011607 BORDETELLA PERTUSSIS / PARAPERTUSSIS - 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 Bordetella 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-04049095160325 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- R-Biopharm AG
- EUDAMED SRN
- DE-MF-000007993
Sources (1)
- EUDAMED 1dd1faff-7d2a-42b1-961e-97ad116ffe57 61 fields · synced Jun 19, 2026