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TST External Fixator System

by Tst Rakor Ve Tibbi̇ Aletler San.ve Ti̇c.ltd.şti̇. EUDAMED

Active European Union

Ref 40564106340Model ULNA RADIUS ROD

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08699931004588 Basic UDI-DIDate17 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Device Name
Umef Ulna-Radius Rod Carbon FIBER6X340 Mm
Model / Reference
ULNA RADIUS ROD, 40564106340
Primary DI / UDI-DI
08699931004588
Basic UDI-DI
B-08699931004588
EMDN Code
P0912040102 Axial bone fixation systems
Device Class
Class IIb
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000017767

Other devices from Tst Rakor Ve Tibbi̇ Aletler San.ve Ti̇c.ltd.şti̇.

See all devices from Tst Rakor Ve Tibbi̇ Aletler San.ve Ti̇c.ltd.şti̇. →

Properties

  • Implantable

Other properties (12)

  • Sterile: 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