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RIDA®Xplore System

EUDAMED

Class A (EU MDR)

Ref 96521

by AusDiagnostics Pty Ltd

Identity

Trade Name
RIDA®Xplore System EUDAMED
Device Name
Thermal cycler nucleic acid amplification analyser IVD, laboratory, semi-automated EUDAMED
Model / Reference
96521 EUDAMED

Identifiers

Primary DI / UDI-DI
09343044005848 EUDAMED
Basic UDI-DI
93430440W02039006V6 EUDAMED
Direct Marketing DI
09343044005848 EUDAMED
EMDN Code
W02039006 DNA THERMAL CYCLERS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Malta 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

Yes

EUDAMED

RIDA®Xplore System by AusDiagnostics Pty Ltd — 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
AU-MF-000020558
Authorised Representative
R-Biopharm AG DE-AR-000050025

Sources (1)

  • EUDAMED 1fa1d8de-8202-40a4-b00a-184a31226e3e 61 fields · synced Jul 10, 2026