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SpeediBag

EUDAMED

Class I (EU MDR)

Ref 28592

by Coloplast A/S

Identity

Trade Name
SpeediBag EUDAMED
Device Name
SpeediBag non-sterile non-drainable EUDAMED
Model / Reference
28592 EUDAMED

Identifiers

Primary DI / UDI-DI
05708932432191 EUDAMED
Basic UDI-DI
57089322978549K EUDAMED
Unit of Use DI
05701780202206 EUDAMED
EMDN Code
A06030301 URINE COLLECTION BAGS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Liechtenstein 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

SpeediBag 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 1153b4da-f206-4bdf-80a6-a63e77941dd4 61 fields · synced Jun 18, 2026