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Assura

EUDAMED

Class I (EU MDR)

Ref 12705

by Coloplast A/S

Identity

Trade Name
Assura EUDAMED
Device Name
Assura/Alterna (Original) ostomy baseplate convex EUDAMED
Model / Reference
12705 EUDAMED

Identifiers

Primary DI / UDI-DI
05701780755450 EUDAMED
Basic UDI-DI
57089322976108M EUDAMED
Unit of Use DI
05701780087780 EUDAMED
EMDN Code
A1002010402 UNIVERSAL PLATES FOR ABDOMINAL STOMA (COLO-, ILEO-, UROSTOMY) WITH INTROFLEX STOMA 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

Assura by Coloplast 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
Coloplast A/S
EUDAMED SRN
DK-MF-000025526

Sources (1)

  • EUDAMED 0c2ca2b3-8964-42e2-bacd-359868b67e95 61 fields · synced May 26, 2026