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Hexafluoruro de azufre para cirugía de desprendimiento de retina y del agujero macular

by S.E. Carburos Metálicos, S.A. Spain EUDAMED

Ref SF6OPHT

EMDN Q02030101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08420219100070 Basic UDI-DIDate16 Sep 2022RegisteredStatusActive

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 22 Oct 2026

Device Name
Sulphur Hexafluoride for Retinal Detachment and Macular Hole Surgery
Model / Reference
SF6OPHT
Primary DI / UDI-DI
08420219100070
Basic UDI-DI
B-08420219100070
EMDN Code
Q02030101 Intraocular fluorinated derivatives
Device Class
Class IIb
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000003117

Other devices from S.E. Carburos Metálicos, S.A.

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Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • 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

Sources (1)

  • EUDAMED ea9ce398-408b-4da6-9c47-4d231d77da60 61 fields · synced 22 Oct 2026