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Danafast Tubular retention bandage

EUDAMED

Class I (EU MDR)

Ref 6050761

by Mediplast AB

Identity

Device Name
Danafast Tubular retention bandage EUDAMED
Danafast Tubular retention bandage, viscose EUDAMED
Model / Reference
6050761 EUDAMED

Identifiers

Primary DI / UDI-DI
07395502042751 EUDAMED
Basic UDI-DI
73955026107115AMZ EUDAMED
Direct Marketing DI
07395502042751 EUDAMED
EMDN Code
M03030201 TUBULAR MESH EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Danafast Tubular retention bandage by Mediplast AB — 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
Mediplast AB
EUDAMED SRN
SE-MF-000000885

Sources (2)

  • EUDAMED 2a2c94b1-ab59-4b1c-a7d0-80b5b5f64976 61 fields · synced Aug 3, 2026
  • EUDAMED e67ae0b9-acbc-4fd2-98d1-bb8b420b5322 61 fields · synced Aug 3, 2026