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Randox Discovery

EUDAMED

Class A (EU MDR)

Ref RDC10000

by Randox Laboratories Limited

Identity

Trade Name
Randox Discovery EUDAMED
Device Name
Randox Discovery EUDAMED
Model / Reference
RDC10000 EUDAMED

Identifiers

Primary DI / UDI-DI
05055273216943 EUDAMED
Basic UDI-DI
50552732ADISCOV018FH EUDAMED
Direct Marketing DI
05055273216943 EUDAMED
EMDN Code
W02050201 MICRO-ARRAY ANALYSERS 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

Randox Discovery 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

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Manufacturer

EUDAMED SRN
XI-MF-000028410

Sources (1)

  • EUDAMED 5ea94ba5-ad41-45f5-a35c-217813a97a0c 61 fields · synced Jun 18, 2026