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Leukocrepe®

EUDAMED

Class I (EU MDR)

Ref 08238-01

by BSN medical GmbH

Identity

Trade Name
Leukocrepe® EUDAMED
Device Name
Leukocrepe® EUDAMED
Model / Reference
08238-01 EUDAMED

Identifiers

Primary DI / UDI-DI
04042809533071 EUDAMED
Basic UDI-DI
4042809400405548J 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
Netherlands 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

Leukocrepe® 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 bb7545d9-aff9-4ad6-9030-116d3156e26a 61 fields · synced Jun 20, 2026