Skip to content

MRI Conditional 5.0mm Guided Locking Hexagonal Head Cannula Cortico-Spongious Screw Stainless Steel 24mm

by HİPOKRAT Tıbbi Malzemeler İmalat ve Pazarlama A.Ş.

Ref 429.8060

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-08698454295619 Basic UDI-DI 08698454295619UDI-DIDate21 Apr 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  • Withdrawn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
Spongioz Screw
Model / Reference
429.8060
Primary DI / UDI-DI
08698454295619
Basic UDI-DI
B-08698454295619
EMDN Code
P09120102 Anchors, tendon and ligament synthesis
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000017246

Other devices from HİPOKRAT Tıbbi Malzemeler İmalat ve Pazarlama A.Ş.

See all devices from HİPOKRAT Tıbbi Malzemeler İmalat ve Pazarlama A.Ş. →

Properties

  • Implantable

Other properties (10)

  • Sterile: 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