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RIDA®Plex S RNA Reservoir

EUDAMED

Class A (EU MDR)

Ref 40731

by AusDiagnostics Pty Ltd

Identity

Trade Name
RIDA®Plex S RNA Reservoir EUDAMED
Device Name
Nucleic acid amplification mastermix reagent IVD EUDAMED
Model / Reference
40731 EUDAMED

Identifiers

Primary DI / UDI-DI
09343044005329 EUDAMED
Basic UDI-DI
93430440W010590010259 EUDAMED
Direct Marketing DI
09343044005329 EUDAMED
EMDN Code
W0105900102 REAGENTS FOR DNA AND/OR RNA AMPLIFICATION AND/OR DETECTION: BACTERIA AND/OR VIRUS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

Yes

EUDAMED

RIDA®Plex S RNA Reservoir 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 6e7bf5f2-61b8-4cd1-ac1a-e0fd9bc0a557 61 fields · synced Jun 19, 2026