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Angiocath

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

Ref ATA0074

EMDN C0104020202

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-8683771504407CF Basic UDI-DIDate27 Dec 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Angiocath Guide Catheter, 6F 120 cm, Judkins Right, Straight
Model / Reference
ATA0074
Primary DI / UDI-DI
D-8683771504407CF
Basic UDI-DI
B-8683771504407CF
EMDN Code
C0104020202 Peripheral embolisation catheters and microcatheters
Device Class
Class III
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 & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 644cf865-3eb9-4d86-9990-96ddf5ef77e6 61 fields · synced 24 Oct 2026