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Dansac

EUDAMED

Class I (EU MDR)

Ref 9232-10

by Dansac A/S

Identity

Trade Name
Dansac EUDAMED
Device Name
1-Piece Drainable Ostomy Pouch, GX EUDAMED
Model / Reference
9232-10 EUDAMED

Identifiers

Primary DI / UDI-DI
05709817532111 EUDAMED
Basic UDI-DI
5709817D02P039S002462 EUDAMED
Unit of Use DI
25709817532115 EUDAMED
EMDN Code
A1001010102 ONE-PIECE COLOSTOMY BAGS FOR NON-RETRACTED STOMA, FLAT, WITH TISSUE COVER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Dansac by Dansac A/S — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Dansac A/S
EUDAMED SRN
DK-MF-000001514

Sources (1)

  • EUDAMED 7d07af73-a2b3-4ee7-bf20-734ba24764cf 61 fields · synced Jun 18, 2026