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Ocufresh

by Blumont Healthcare Ltd EUDAMED 2 variants

Active European Union

Ref 1626 Ocufresh Mist GreyModel EM-1626

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5060148681626VG Basic UDI-DIDate11 Sep 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  • Withdrawn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
Heated Eye Mask
Model / Reference
EM-1626, 1626 Ocufresh Mist Grey
Primary DI / UDI-DI
05060148680743
Basic UDI-DI
5060148681626VG
EMDN Code
M9001 Cryotherapy and thermotherapy devices
Device Class
Class I
Market of Registration
Belgium

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

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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