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HD-035 Hemodialysis Connection-Disconnection set

by Sanus Sağlik Hi̇zmetleri̇ Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Ref HD-035

Active European Union

CE MDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8684072514SNSJA Basic UDI-DI 08681873029484UDI-DIDate21 Oct 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Hemodialysis (Fistula) Connection-Disconnection Sets
Model / Reference
HD-035
Primary DI / UDI-DI
08681873029484
Basic UDI-DI
8684072514SNSJA
EMDN Code
F900201 Temporary hemodialysis catheters and kits
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
TR-MF-000019644

Other devices from Sanus Sağlik Hi̇zmetleri̇ Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • 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