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Leukoplast® elastofix® s

EUDAMED

Class I (EU MDR)

Ref 71641-10

by BSN medical GmbH

Identity

Trade Name
Leukoplast® elastofix® s EUDAMED
Device Name
Elastofix® S / Leukoplast® elastofix® s EUDAMED
Model / Reference
71641-10 EUDAMED

Identifiers

Primary DI / UDI-DI
04042809220940 EUDAMED
Basic UDI-DI
404280940039591AC EUDAMED
EMDN Code
M03030201 TUBULAR MESH EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Leukoplast® elastofix® s by BSN medical GmbH — 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
BSN medical GmbH
EUDAMED SRN
DE-MF-000005787

Sources (1)

  • EUDAMED 8428ab29-d34f-4d35-b220-5bd5a8f1e1bd 61 fields · synced Aug 1, 2026