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Ektal M (GOECP-004)

by Enable Innovations SRL Italy EUDAMED

Ref 050639Model Gocce oculari EC+HA EMDN Q0299

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number80540851218P2 Basic UDI-DIDate13 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030119-01 Supplemented

    Quality management system EU MDR

    Notified body
    ICIM S.P.A. 0425
    Issued
    25 Feb 2026
    Expires
    2 Feb 2030
    Reason
    Add device or group

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Gocce oculari EC+HA
Model / Reference
Gocce oculari EC+HA, 050639
Primary DI / UDI-DI
08054085122500
Basic UDI-DI
80540851218P2
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIb
Market of Registration
Portugal

Manufacturer details

EUDAMED SRN
IT-MF-000026066

Other devices from Enable Innovations SRL

See all devices from Enable Innovations SRL →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 08054085122500|80540851218P2 61 fields · synced 24 Oct 2026