← Back to catalogue

Rotor-Gene Q MDx 5Plex

EUDAMED

Class A (EU MDR)

Ref 9002020

by QIAGEN GmbH

Identity

Trade Name
Rotor-Gene Q MDx 5Plex EUDAMED
Device Name
Rotor-Gene Q MDx EUDAMED
Model / Reference
9002020 EUDAMED

Identifiers

Primary DI / UDI-DI
04053228022077 EUDAMED
Basic UDI-DI
4053228IRGQ000000000001QQ EUDAMED
Direct Marketing DI
04053228022077 EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria 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

Category: Nucleic acid sample preparation instrument IVD

Rotor-Gene Q MDx 5Plex by QIAGEN GmbH — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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

Manufacturer

Manufacturer
QIAGEN GmbH
EUDAMED SRN
DE-MF-000004949

Sources (1)

  • EUDAMED ab2eec1d-3e08-433e-b711-aee121c98189 61 fields · synced Jul 28, 2026