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Vitrectomy Dual Cutter 23G - Connector A-A

by Aktive SRL Italy EUDAMED

Ref AK-0236/AA2Model Vitrectomy Cutter/Vitrectomo

EMDN Q020499

Regulatory status

as of 24 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
  • 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 · synced 24 Oct 2026

Device Name
Vitrectomy Cutter/Vitrectomo
Model / Reference
Vitrectomy Cutter/Vitrectomo, AK-0236/AA2
Primary DI / UDI-DI
08058340220895
Basic UDI-DI
8052276FT0003HJ
Unit of Use DI
08056477556665
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 & 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 b7dffb06-1495-4e34-90b0-659e18139082 61 fields · synced 24 Oct 2026