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Cutimed® Siltec®

by BSN medical GmbH EUDAMED

Active European Union

Ref 73285-07

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40428094004348399 Basic UDI-DIDate2 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Cutimed® Siltec® / Leukoplast® Cutimed ®Siltec®
Model / Reference
73285-07
Primary DI / UDI-DI
04042809556742
Basic UDI-DI
40428094004348399
Unit of Use DI
04042809703542
EMDN Code
M04040601 Polyurethane dressings, non-combined
Device Class
Class IIb
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
DE-MF-000005787

Other devices from Bsn Medical, Inc.

See all devices from Bsn Medical, Inc. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No