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Alterna

EUDAMED

Class I (EU MDR)

Ref 017750

by Coloplast A/S

Identity

Trade Name
Alterna EUDAMED
Device Name
Assura/Alterna (Original) ostomy baseplate EUDAMED
Model / Reference
017750 EUDAMED

Identifiers

Primary DI / UDI-DI
05701780779876 EUDAMED
Basic UDI-DI
570893229760994 EUDAMED
Unit of Use DI
05701780016476 EUDAMED
EMDN Code
A1002010401 UNIVERSAL PLATES FOR ABDOMINAL STOMA (COLO-, ILEO-, UROSTOMY) WITH NON-INTROFLEX STOMA EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Alterna 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 f4080c44-df82-48ac-8095-19331a2696ec 61 fields · synced May 29, 2026