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Cyborg

by Duru Grup Tibbi̇ Ürünler Sanayi̇ Ve Ti̇caret A.Ş. 74 variants

Ref 585

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08681990205853 Basic UDI-DI 08681990205853UDI-DIDate9 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Femoral Bipolar Baş (Shell + İnsert) -CoCrCo + UHMWPE - Ø28 - sz58
Model / Reference
585
Primary DI / UDI-DI
08681990205853
Basic UDI-DI
B-08681990205853
EMDN Code
P0908040503 Hip prostheses, bi-articular cups
Device Class
Class III
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000029561

Other devices from Duru Grup Tibbi̇ Ürünler Sanayi̇ Ve Ti̇caret A.Ş.

See all devices from Duru Grup Tibbi̇ Ürünler Sanayi̇ Ve Ti̇caret A.Ş. →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • 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