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Infusion set Tanaphar

by Tanaphar Joint Stock Company 3 variants

Ref DTD.KK.TNP; DTD.KT.TNP; DTD.KB1.TNP; DTD.KB2.TNP - Bag

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

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/MDD NumberB-08936043817690 Basic UDI-DI 08936043817690UDI-DIDate9 Oct 2026RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDD Withdrawn

Specification

EUDAMED

Device Name
Infusion set for single use
Model / Reference
DTD.KK.TNP, DTD.KT.TNP, DTD.KB1.TNP, DTD.KB2.TNP - Bag
Primary DI / UDI-DI
08936043817690
Basic UDI-DI
B-08936043817690
EMDN Code
A03040199 Infusion kits (with or w/o pump), single-use - other
Device Class
Class IIa

Manufacturer details

EUDAMED SRN
VN-MF-000012680
Authorised representative
Obelis s.a. BE-AR-000000106

Properties

  • Sterile
  • Administering Medicine

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No