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Klini Flex 10cmx4m white KLP

by KliniBand Kft. EUDAMED

Active European Union

Ref KB00310100040

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59991482KB03WN Basic UDI-DIDate11 Jul 2025RegisteredStatusActive

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  • Withdrawn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
Klini Flex
Model / Reference
KB00310100040
Primary DI / UDI-DI
05999148202931
Basic UDI-DI
59991482KB03WN
EMDN Code
M0303010101 Elastic fixing bandages, non-adhesive, extensible in one direction
Device Class
Class I
Market of Registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000047539

From the manufacturer

Manufacturer's product page: Klini Flex

Other devices from KliniBand Kft.

See all devices from KliniBand 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