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Benda previlast s/clip 4mx8cm

by Medinovitas Kft EUDAMED

Active European Union

Ref LAS040081Model Benda elastica previcrepe

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number599957142M0303010101Z5 Basic UDI-DIDate15 Jul 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Benda elastica previcrepe
Model / Reference
Benda elastica previcrepe, LAS040081
Primary DI / UDI-DI
05999571422050
Basic UDI-DI
599957142M0303010101Z5
EMDN Code
M0303010101 Elastic fixing bandages, non-adhesive, extensible in one direction
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
HU-MF-000007416

Other devices from Medinovitas Kft

See all devices from Medinovitas Kft →

Properties

Show properties
Other properties (13)
  • Sterile: No
  • 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