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SenSura Flex

EUDAMED

Class I (EU MDR)

Ref 11828

by Coloplast A/S

Identity

Trade Name
SenSura Flex EUDAMED
Device Name
SenSura Flex urostomy bag 2-piece EUDAMED
Model / Reference
11828 EUDAMED

Identifiers

Primary DI / UDI-DI
05708932396752 EUDAMED
Basic UDI-DI
57089322975749A EUDAMED
Unit of Use DI
05701780074803 EUDAMED
EMDN Code
A10020402 UROSTOMY BAGS FOR TWO-PART SYSTEMS, WITH TISSUE COVER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

SenSura Flex 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 96ad7621-462a-4094-9347-00f1ae460fa3 61 fields · synced May 21, 2026