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C3F8 - Flacone 50cc - Puro

by Micromed srl EUDAMED

Active European Union

Ref EG-C3F8P

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0007230223 Date12 May 2023IssuedStatusActive expires 7 Mar 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • CSQ0007230223 Supplemented

    Quality management system EU MDR

    Issued
    12 May 2023
    Expires
    7 Mar 2028
    Reason
    Add device or group
  • CVD000323 Issued

    Technical documentation EU MDR

    Issued
    8 Mar 2023
    Expires
    7 Mar 2028

Specification

EUDAMED

Device Name
Microgas
Model / Reference
EG-C3F8P
Primary DI / UDI-DI
08033757390386
Basic UDI-DI
803375739MICROGAS97
EMDN Code
Q02030101 Intraocular fluorinated derivatives
Device Class
Class IIb
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000009198

Other devices from Micromed srl

See all devices from Micromed srl →

Properties

  • Sterile
  • Implantable

Other properties (12)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Sutures: 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