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Pedesente

by Doğsan Tibbi̇ Malzeme Sanayi̇ A.Ş. 111 variants

Ref D5300

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-08698147925571 Basic UDI-DI 08698147925571UDI-DIDate18 May 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
D5300
Primary DI / UDI-DI
08698147925571
Basic UDI-DI
B-08698147925571
EMDN Code
H010101010101, H010101010102
Device Class
Class III
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000016026

Other devices from Doğsan Tibbi̇ Malzeme Sanayi̇ A.Ş.

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    Class III

  • Politer

    Class III

  • Propilen

    Class III

  • Xnat-Pedesente

    Class III

  • İpek

    Class IIb

  • PEGELAK rapid

    Class III

See all devices from Doğsan Tibbi̇ Malzeme Sanayi̇ A.Ş. →

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