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Teknomek

by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ. 357 variants

Ref VKIVK115

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-08680548917033 Basic UDI-DIDate18 Mar 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  • Withdrawn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
Intravitreal Injection Kit
Model / Reference
VKIVK115
Primary DI / UDI-DI
08680548917033
Basic UDI-DI
B-08680548917033
EMDN Code
Q021113 Ophthalmic surgery instrument kits, single-use
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018462

Other devices from TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ.

See all devices from TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ. →

Properties

  • Sterile
  • Contains Latex
  • Administering Medicine

Other properties (8)

  • Implantable: No
  • Reusable: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No