← Back to catalogue

Oncomine™ Dx Express Test FFPE DNA Control

EUDAMED

Class IVD General (EU MDR)

Ref A50834 (A52167)

by Life Technologies Corporation

Identity

Trade Name
Oncomine™ Dx Express Test FFPE DNA Control EUDAMED
Device Name
Oncomine™ Dx Express Test FFPE DNA Control, a part of Ion Torrent™ Oncomine™ Dx Express Test EUDAMED
Model / Reference
A50834 (A52167) EUDAMED

Identifiers

Primary DI / UDI-DI
D-USMF000023929A508347V EUDAMED
Basic UDI-DI
B-USMF000023929A508347V EUDAMED
EMDN Code
W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

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

Oncomine™ Dx Express Test FFPE DNA Control by Life Technologies Limited — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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

Manufacturer

EUDAMED SRN
US-MF-000023929
Authorised Representative
Life Technologies Europe B.V. NL-AR-000021890

Sources (1)

  • EUDAMED 5d523e13-7652-4204-b061-af79a767ea85 61 fields · synced Jun 19, 2026