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Duoten

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

Ref CA0041

EMDN C010402020302

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-86824086301829G Basic UDI-DIDate3 Jan 2024RegisteredStatusActive

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 23 Oct 2026

Device Name
Duoten Non-Adhesive Embolization Agent (1cc)
Model / Reference
CA0041
Primary DI / UDI-DI
D-86824086301829G
Basic UDI-DI
B-86824086301829G
EMDN Code
C010402020302 Embolisation fluids
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
  • Implantable
Other properties (9)
  • 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 c3c016c3-0fd1-48b4-b37a-d29d63a38628 61 fields · synced 23 Oct 2026