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İnvamed

by İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş. EUDAMED

Active European Union

Ref CA0140

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-86814100669966E Basic UDI-DIDate29 Jan 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
MicroDelivery Catheter,Laser Light Guided, ID: 0,7 mm,100 cm, with Guidewire
Model / Reference
CA0140
Primary DI / UDI-DI
D-86814100669966E
Basic UDI-DI
B-86814100669966E
EMDN Code
C0104020202 Peripheral embolisation catheters and microcatheters
Device Class
Class IIb
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000019963

Other devices from İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş.

See all devices from İnvamed Sağlik İlaç Sanayi̇ Ve Ti̇caret A.Ş. →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No