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TST Anatomic Pressfit System

by Tst Rakor Ve Tibbi̇ Aletler San.ve Ti̇c.ltd.şti̇. 53 variants

Ref 11224000052Model PRESS FIT CUP

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-08680858420421 Basic UDI-DI 08680858420421UDI-DIDate10 Jun 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  • Withdrawn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
Anat. Press Fit Cup Pc & Ha Coated 52 Mm
Model / Reference
PRESS FIT CUP, 11224000052
Primary DI / UDI-DI
08680858420421
Basic UDI-DI
B-08680858420421
EMDN Code
P090803010201 Primary implant uncemented metal acetabular cups
Device Class
Class III
EU 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

  • Sterile
  • Implantable

Other properties (11)

  • 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