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Optrex Double Action Rehydrating Eye Drops Dry Eyes

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

Ref DT/01/DT009Model DT/01/DT/009

Active European Union

CE MDR

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803395976DT01DT009ZR Basic UDI-DI 05011417590942UDI-DIDate14 Apr 2023RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
DT/01/DT/009, DT/01/DT009
Primary DI / UDI-DI
05011417590942
Basic UDI-DI
803395976DT01DT009ZR
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
  • CMR Substance

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No