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Alterna

EUDAMED

Class I (EU MDR)

Ref 13840

by Coloplast A/S

Identity

Trade Name
Alterna EUDAMED
Device Name
Assura/Alterna (New Generation) ostomy bag 1-piece open EUDAMED
Model / Reference
13840 EUDAMED

Identifiers

Primary DI / UDI-DI
05701780809733 EUDAMED
Basic UDI-DI
570893229754899 EUDAMED
Unit of Use DI
05701780095020 EUDAMED
EMDN Code
A1001010102,A1001020102 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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 b2fe6cbd-96cf-4d38-b951-7cff04ca561d 61 fields · synced May 29, 2026