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Ocufresh-C Lubricating Eye Drops

by Blumont Healthcare Ltd EUDAMED

Active European Union EUDAMED: not on the EU market

Ref 1606AModel ED-1606

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5060148681606VA Basic UDI-DIDate13 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

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

Device Name
Hypromellose 0.3% eye drops (with SOC)
Model / Reference
ED-1606, 1606A
Primary DI / UDI-DI
05060148681252
Basic UDI-DI
5060148681606VA
Direct Marketing DI
05060148681252
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
GB-MF-000010003
Authorised representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Other devices from Blumont Healthcare Ltd

See all devices from Blumont Healthcare Ltd →

Properties

  • Sterile
  • CMR Substance
  • Endocrine Disruptor

Other properties (10)

  • Implantable: 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