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Venaporta

by Venaporta Tibbi Malzemeler Imalat Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi EUDAMED

Active European Union

Ref 519567Model Felt 50 mm x 7 cm (1 pcs / pouch)

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08699142519567 Basic UDI-DIDate15 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
Felt 50 mm x 7 cm (1 pcs / pouch), 519567
Primary DI / UDI-DI
08699142519567
Basic UDI-DI
B-08699142519567
EMDN Code
H900302 Suture felts
Device Class
Class III
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000021260

Other devices from Venaporta Tibbi Malzemeler Imalat Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi

See all devices from Venaporta Tibbi Malzemeler Imalat Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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