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Coloplast

EUDAMED

Class I (EU MDR)

Ref 140100

by Coloplast A/S

Identity

Trade Name
Coloplast EUDAMED
Generic Name
DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED
Device Name
Coloplast Fistula Bed Drainage Bags EUDAMED
Model / Reference
140100 EUDAMED

Identifiers

Primary DI / UDI-DI
05708932266741 EUDAMED
Basic UDI-DI
5708932117046129HX EUDAMED
Unit of Use DI
05701780100908 EUDAMED
EMDN Code
A99 DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED

Classification

Legislation / Framework
MDR (REGULATION (EU) 2017/745 on medical devices) EUDAMED
Market of Registration
France 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

Coloplast by Coloplast A/S (devices for administration, withdrawal and collection - other) — 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 68 fields · synced May 23, 2026