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Mesoft

EUDAMED

Class I (EU MDR)

Ref 157000

by Mölnlycke Health Care AB

Identity

Trade Name
Mesoft EUDAMED
Device Name
Mesoft Non Sterile EUDAMED
Model / Reference
157000 EUDAMED

Identifiers

Primary DI / UDI-DI
07332430905215 EUDAMED
Basic UDI-DI
733243000000000026JS EUDAMED
EMDN Code
M0202030102 NON-WOVEN GAUZE PADS, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE 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

Mesoft 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 76556de0-aeb0-4683-b36e-95d6256838cf 61 fields · synced Oct 11, 2026