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Vanocathe

by iLife Medical Devices Pvt Ltd EUDAMED

Active European Union

Ref 906.06.01.02Model Extension Tube

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number890603910906FZ Basic UDI-DIDate18 May 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
Extension Tube, 906.06.01.02
Primary DI / UDI-DI
08906039100914
Basic UDI-DI
890603910906FZ
EMDN Code
A03020199 Extensions - other
Device Class
Class IIa
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
IN-MF-000014372
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from iLife Medical Devices Pvt Ltd

See all devices from iLife Medical Devices Pvt Ltd →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

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