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Danafast Tubular retention bandage

EUDAMED

Class I (EU MDR)

Ref 6050751

by Mediplast AB

Identity

Device Name
Danafast Tubular retention bandage EUDAMED
Danafast Tubular retention bandage, viscose EUDAMED
Model / Reference
6050751 EUDAMED

Identifiers

Primary DI / UDI-DI
07395502030840 EUDAMED
Basic UDI-DI
73955026107115AMZ EUDAMED
Direct Marketing DI
07395502030840 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 b80ec3e3-17d1-433f-b425-9e62ee643ff7 61 fields · synced Jul 24, 2026
  • EUDAMED b6c9e603-603d-435a-b0d5-0c44fa743a10 61 fields · synced Jul 24, 2026