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INDERMIL Flexifuze

by Connexicon Medical Ltd Ireland EUDAMED

Ref CM001

EMDN H90010102

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number539153136CM0012A Basic UDI-DIDate17 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
INDERMIL Flexifuze
Model / Reference
CM001
Primary DI / UDI-DI
05391531360011
Basic UDI-DI
539153136CM0012A
Unit of Use DI
05391531360004
EMDN Code
H90010102 Synthetic glues
Device Class
Class IIa
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
IE-MF-000023506

Other devices from Connexicon Medical Ltd

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 48a4d939-d057-4811-9141-959ce64f50bc 61 fields · synced 22 Oct 2026