Skip to content

Dexvur

by Ekspo Farma İlaç Medi̇kal San. ve Ti̇c. Ltd. Şti̇. Türkiye EUDAMED

Ref EKS-1

EMDN A02010799

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682874230015 Basic UDI-DIDate2 Jun 2026RegisteredStatusActive

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
Injectable Gel for Treatments of Vesicoureteral Reflux (Vur)
Model / Reference
EKS-1
Primary DI / UDI-DI
08682874230015
Basic UDI-DI
B-08682874230015
EMDN Code
A02010799 Prefilled syringes - other
Device Class
Class III
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000040218

Other devices from Ekspo Farma İlaç Medi̇kal San. ve Ti̇c. Ltd. Şti̇.

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 53644de8-71c0-44f2-94f6-801e4daf6ecd 61 fields · synced 24 Oct 2026