Identity
- Trade Name
- RX modena EUDAMED
- Device Name
- RX modena EUDAMED
- Model / Reference
- RX9000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05055273214963 EUDAMED
- Basic UDI-DI
- 50552732AMODENA033DB EUDAMED
- Direct Marketing DI
- 05055273214963 EUDAMED
- EMDN Code
- W0201010106 CHEMISTRY ANALYSERS - MODERATE ROUTINE (with ISE mode test/h > 400 and <= 800) EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Northern Ireland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
Yes
EUDAMED
New Device
No
EUDAMED
RX modena by Randox Laboratories Limited — Class A — 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 | 50552732AMODENA033DB | Class A | Active |
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Manufacturer
- Manufacturer
- Randox Laboratories Limited
- EUDAMED SRN
- XI-MF-000028410
Sources (1)
- EUDAMED 6bc2a55b-1245-4faa-bfea-18ec7909521d 61 fields · synced Jul 18, 2026