Identity
- Trade Name
- RX daytona plus (without ISE) EUDAMEDRX daytona plus FDA UDI
- Generic Name
- Multiple clinical chemistry analyser IVD, laboratory FDA UDI
- Device Name
- RX daytona plus EUDAMEDThe Randox RX daytona plus without ISE is a fully automated, random access, clinical chemistry analyser complete with dedicated analyser software. FDA UDI
- Model / Reference
- RX4041 EUDAMEDFDA UDI
- Description
- The Randox RX daytona plus without ISE is a fully automated, random access, clinical chemistry analyser complete with dedicated analyser software. FDA UDI
Identifiers
- Catalog Number
- RX4041 FDA UDI
- Primary DI / UDI-DI
- 05055273207781 EUDAMEDFDA UDI
- Basic UDI-DI
- 50552732ADAYPLU015HS EUDAMED
- Direct Marketing DI
- 05055273207781 EUDAMED
- FDA Product Code
- JJE FDA UDI
- EMDN Code
- W0201010101 CHEMISTRY ANALYSERS - LOW ROUTINE (Random access without ISE mode test/h <= 400) EUDAMED
- GMDN Term
- Multiple clinical chemistry analyser IVD, laboratory FDA UDI
Classification
- Device Class
- Class A EUDAMEDClass I FDA UDI
- Regulation Number
- 862.2160 FDA UDI
- Market of Registration
- Northern Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
RX daytona plus (without ISE) by Randox Laboratories Limited — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 50552732ADAYPLU015HS | Class A | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class A | Pending data |
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Manufacturer
- Manufacturer
- Randox Laboratories Limited
- EUDAMED SRN
- XI-MF-000028410
Sources (2)
- EUDAMED 8ead3ea4-0a4a-45b4-9ecc-9f9ab241504b 61 fields · synced Jul 12, 2026
- FDA UDI 2f64c290-aa9a-44ea-8ea1-bd1b3aa51fdc 35 fields · synced May 29, 2026