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Vitrectomy Cutter 27G - Connector A-C

by Aktive SRL EUDAMED

Active European Union

Ref AK-0297/ACModel Vitrectomy Cutter/Vitrectomo

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberEPT 0477.MDR.22/5010.1 Date30 Aug 2023IssuedStatusActive expires 13 Dec 2027

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  • Withdrawn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)
  • EPT 0477.MDR.22/5010.1 Reissued

    Quality management system EU MDR

    Notified body
    Notified body 0477
    Issued
    30 Aug 2023
    Expires
    13 Dec 2027

Specification

EUDAMED

Device Name
Vitrectomy Cutter/Vitrectomo
Model / Reference
Vitrectomy Cutter/Vitrectomo, AK-0297/AC
Primary DI / UDI-DI
08052276019363
Basic UDI-DI
8052276FT0003HJ
Unit of Use DI
08056477555026
EMDN Code
Q020499 Vitrectomy devices - other
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000007813

Other devices from Aktive SRL

See all devices from Aktive SRL →

Properties

Show properties
  • 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