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Safeline Kit Dialysis Set Hd End I

by Su Biyomedikal Sistemler ve Sağlık Hizmetleri Sanayi ve Ticaret Anonim Şirketi 3 variants

Ref W061423102_3720

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682780977998 Basic UDI-DI 08682780977998UDI-DIDate13 Jul 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Dialysis Set Hd
Model / Reference
W061423102_3720
Primary DI / UDI-DI
08682780977998
Basic UDI-DI
B-08682780977998
EMDN Code
F0303 Haemodialysis kits
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
TR-MF-000017528

Other devices from Su Biyomedikal Sistemler ve Sağlık Hizmetleri Sanayi ve Ticaret Anonim Şirketi

See all devices from Su Biyomedikal Sistemler ve Sağlık Hizmetleri Sanayi ve Ticaret Anonim Şirketi →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • 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