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by C.O.C. Farmaceutici S.R.L. EUDAMED

Withdrawn Not intended for the EU market

Ref DT/01/DT/010

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803395976DT01DT010ZA Basic UDI-DIDate14 Apr 2023RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Withdrawn

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.

Specification

EUDAMED

Model / Reference
DT/01/DT/010
Primary DI / UDI-DI
08033959760550
Basic UDI-DI
803395976DT01DT010ZA
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IT-MF-000019321

Other devices from C.O.C. Farmaceutici S.R.L.

See all devices from C.O.C. Farmaceutici S.R.L. →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • 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