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RX daytona plus (with ISE)

EUDAMEDFDA UDI

Class A (EU MDR)

Ref RX4040

by Randox Laboratories Limited

Identity

Trade Name
RX daytona plus (with ISE) EUDAMED
RX daytona plus FDA UDI
Generic Name
Multiple clinical chemistry analyser IVD, laboratory FDA UDI
Device Name
RX daytona plus EUDAMED
The Randox RX daytona plus with ISE is a fully automated, random access, clinical chemistry analyser complete with dedicated analyser software. FDA UDI
Model / Reference
RX4040 EUDAMEDFDA UDI
Description
The Randox RX daytona plus with ISE is a fully automated, random access, clinical chemistry analyser complete with dedicated analyser software. FDA UDI

Identifiers

Catalog Number
RX4040 FDA UDI
Primary DI / UDI-DI
05055273207774 EUDAMEDFDA UDI
Basic UDI-DI
50552732ADAYPLU015HS EUDAMED
Direct Marketing DI
05055273207774 EUDAMED
FDA Product Code
JJE FDA UDI
EMDN Code
W0201010105 CHEMISTRY ANALYSERS - LOW ROUTINE (with ISE mode test/h <= 400) EUDAMED
GMDN Term
Multiple clinical chemistry analyser IVD, laboratory FDA UDI

Classification

Device Class
Class A EUDAMED
Class 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 (with 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
XI-MF-000028410

Sources (2)

  • EUDAMED 34f89ee7-03aa-4d66-853f-fb4e5c1f8bc9 61 fields · synced Jun 18, 2026
  • FDA UDI 34415135-8e31-4fd9-9276-c5ac62dbf179 35 fields · synced May 30, 2026