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IDK TREx®

EUDAMED

Class A (EU MDR)

Ref K 6993

by Immundiagnostik AG

Identity

Trade Name
IDK TREx® EUDAMED
Device Name
IDK TREx® EUDAMED
Model / Reference
K 6993 EUDAMED

Identifiers

Primary DI / UDI-DI
04050598015968 EUDAMED
Basic UDI-DI
4050598DVAuto5H EUDAMED
Direct Marketing DI
04050598015968 EUDAMED
EMDN Code
W05019001 FAECES COLLECTION DEVICES 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

No

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

IDK TREx® by Immundiagnostik AG — 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

Manufacturer
Immundiagnostik AG
EUDAMED SRN
DE-MF-000020905

Sources (1)

  • EUDAMED bf062ed4-af0f-4c8f-aa4d-f1a9ca2298c6 61 fields · synced Jul 9, 2026