Skip to content

Kit IOL Mini 4 Ready +20.50D

by SIFI S.p.A. EUDAMED

Active European Union

Ref S7560CZModel S7560CZP00003

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8027864SIFIMDF03MZ Basic UDI-DIDate14 Sep 2026RegisteredStatusActive

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  • Withdrawn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)
  • 028-00-04-MDR Supplemented

    Technical documentation EU MDR

    Notified body
    ITALCERT SRL 0426
    Issued
    1 Sep 2026
    Expires
    31 Aug 2028
    Reason
    Add device or group

Specification

EUDAMED

Trade Name
Kit IOL Mini 4 Ready +20.50D
Kit IOL Mini 4 Ready +25.50D
Kit IOL Mini 4 Ready +22.50D
IOL Mini 4 Ready +20.50D
Kit IOL Mini 4 Ready +21.50D
Kit IOL Mini 4 Ready +27.50D
Kit IOL Mini 4 Ready +24.50D
Device Name
Mini 4 Ready (Kit)
Mini 4 Ready (IOL)
Model / Reference
S7560CZ, S7560CZP00003
Primary DI / UDI-DI
08027864082586, 08027864082685, 08027864082623, 08027864061833, 08027864082609, 08027864082722, 08027864082661
Direct Marketing DI
08027864061833
Market of Registration
Italy
Medical Purpose
MINI 4 Ready aspheric IOLs are intended for primary implantation for visual correction of aphakia in adult patients (≥ 18 years old) after removal of a cataractous lens. These implants must be positioned within the capsular bag.

Manufacturer details

EUDAMED SRN
IT-PR-000021264

Other devices from SIFI S.p.A.

See all devices from SIFI S.p.A. →