Skip to content

NIKA-Mull Haft weiss 12 cm x 20 m kohäsive, elastische Fixierbinde

by KliniBand Kft.

Ref 902012

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59991482KB101RT Basic UDI-DI 05999148225381UDI-DIDate27 Jun 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Klini Crepp Haft
Model / Reference
902012
Primary DI / UDI-DI
05999148225381
Basic UDI-DI
59991482KB101RT
EMDN Code
M0303010201 Elastic fixing bandages, self-adhesive, extensible in one direction
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
HU-MF-000047539

Other devices from KliniBand Kft.

See all devices from KliniBand Kft. →

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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