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93915GM

by AMO Ireland Ireland EUDAMED

Ref 93915GM

EMDN Q0299

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-IEMF0000137040000644F Basic UDI-DIDate21 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
93915GM
Primary DI / UDI-DI
D-IEMF0000137040000644F
Basic UDI-DI
B-IEMF0000137040000644F
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIb
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
IE-MF-000013704

Other devices from AMO Ireland

See all devices from AMO Ireland →

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 52fbee9b-c73a-4af2-b18a-13114a4459c7 61 fields · synced 24 Oct 2026