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Zi̇med Medi̇kal San Ve Ti̇c.ltd.şti̇

by Zimed Medikal Sanayi ve Ticaret Limited Şirketi 322 variants

Ref 7102-0030

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-8699131697825GZ Basic UDI-DI D-8699131697825GZUDI-DIDate14 Mar 2022RegisteredStatusActive

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  • Withdrawn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
ACETABULAR SCREW 30 mm (TITANIUM)
Model / Reference
7102-0030
Primary DI / UDI-DI
D-8699131697825GZ
Basic UDI-DI
B-8699131697825GZ
EMDN Code
P0908030499 Hip prostheses acetabular inserts - other
Device Class
Class III
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
TR-MF-000015401

Other devices from Zimed Medikal Sanayi ve Ticaret Limited Şirketi

See all devices from Zimed Medikal Sanayi ve Ticaret Limited Şirketi →

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