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Vanocathe Safety

by iLife Medical Devices Pvt Ltd EUDAMED

Active European Union

Ref 901.48.06.08Model Intravenous Cannula/Catheter (with/ without safety feature)

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number890603910901FP Basic UDI-DIDate7 Nov 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  • Withdrawn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

Model / Reference
Intravenous Cannula/Catheter (with/ without safety feature), 901.48.06.08
Primary DI / UDI-DI
08906039102352
Basic UDI-DI
890603910901FP
EMDN Code
C0101010201 Peripheral i.v. catheters, with safety systems, with injection valves
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

Show properties
  • 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