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Genexus™ Dx Cartridge

EUDAMED

Class A (EU MDR)

Ref A50865 (A50432)

by Life Technologies Corporation

Identity

Trade Name
Genexus™ Dx Cartridge EUDAMED
Device Name
Ion Torrent™ Genexus™ Dx Sequencing Kit, a part of Ion Genexus™ Dx Reagents and Consumables EUDAMED
Model / Reference
A50865 (A50432) EUDAMED

Identifiers

Primary DI / UDI-DI
10190302017527 EUDAMED
Basic UDI-DI
0190302A50432RC EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

No

EUDAMED

Genexus™ Dx Cartridge by Life Technologies 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
US-MF-000023929
Authorised Representative
Life Technologies Europe B.V. NL-AR-000021890

Sources (1)

  • EUDAMED 44b381b1-7663-47e9-aa2a-d15effce1004 61 fields · synced Jun 18, 2026