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Venaporta

by Venaporta Tibbi Malzemeler Imalat Ithalat Ihracat Sanayi Ve Ticaret Limited Sirketi 910 variants

Ref 501586

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08699142501586 Basic UDI-DI 08699142501586UDI-DIDate23 Aug 2023RegisteredStatusActive

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.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Kardiyovasküler Felt 10x10 cm
Model / Reference
501586
Primary DI / UDI-DI
08699142501586
Basic UDI-DI
B-08699142501586
EMDN Code
H900302 Suture felts
Device Class
Class III
EU 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 (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