Identity
- Device Name
- RIDA®QUICK IFX Monitoring EUDAMED
- Model / Reference
- GP3041 EUDAMEDGN3041 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04049095070174 EUDAMED04049095070167 EUDAMED
- Basic UDI-DI
- 4049095GN30410000AN EUDAMED
- EMDN Code
- W0102080701 INFLIXIMAB EUDAMED
Classification
- Device Class
- Class C 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
New Device
No
EUDAMED
RIDA®QUICK IFX Monitoring by R-Biopharm AG — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 4049095GN30410000AN | Class C | Active |
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Manufacturer
- Manufacturer
- R-Biopharm AG
- EUDAMED SRN
- DE-MF-000007993
Sources (2)
- EUDAMED f86fd8c1-a087-4d90-84b3-5f64414941b8 61 fields · synced Jul 9, 2026
- EUDAMED 21c28b64-43a4-402b-869f-99c91a52eb7e 61 fields · synced May 18, 2026