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Elastofix®

EUDAMED

Class I (EU MDR)

Ref 02142-00

by BSN medical GmbH

Identity

Trade Name
Elastofix® EUDAMED
Device Name
Elastofix® / Leukoplast® elastofix® EUDAMED
Model / Reference
02142-00 EUDAMED

Identifiers

Primary DI / UDI-DI
04042809039931 EUDAMED
Basic UDI-DI
404280940036778A9 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

Elastofix® 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 29427855-b35d-41df-9ee8-0ccb9fa8169b 61 fields · synced Jul 14, 2026