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Idylla™ CDx MSI Test

EUDAMED

Class C (EU MDR)

Ref A0220/6

by Biocartis NV

Identity

Trade Name
Idylla™ CDx MSI Test EUDAMED
Device Name
Idylla™ CDx MSI Test EUDAMED
Model / Reference
A0220/6 EUDAMED

Identifiers

Primary DI / UDI-DI
15415219001328 EUDAMED
Basic UDI-DI
5415219A0220BV EUDAMED
Unit of Use DI
05415219001321 EUDAMED
EMDN Code
W01060214 COLORECTAL CANCER (MSI-H / DMMR) EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Belgium 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

Yes

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Idylla™ CDx MSI Test by Biocartis NV — Class C — 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
Biocartis NV
EUDAMED SRN
BE-MF-000003661

Sources (1)

  • EUDAMED efc6beaf-87eb-4581-b343-b86a6ab7063c 61 fields · synced Jun 20, 2026