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Tubigrip

EUDAMED

Class I (EU MDR)

Ref 1439

by Mölnlycke Health Care AB

Identity

Trade Name
Tubigrip EUDAMED
Device Name
Tubigrip EUDAMED
Model / Reference
1439 EUDAMED

Identifiers

Primary DI / UDI-DI
07333350102111 EUDAMED
Basic UDI-DI
733243000000000063JY EUDAMED
EMDN Code
M030402010101 ELASTIC SUPPORT BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION, HIGH EXTENSIBILITY 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

Yes

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

Tubigrip by Mölnlycke Health Care 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

EUDAMED SRN
SE-MF-000014042

Sources (1)

  • EUDAMED e8da805c-49b8-4c81-bec1-4a6878377bd5 61 fields · synced Oct 8, 2026