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SIFI S.p.A.

Italy Last updated 17 Sep 2026

Devices
2,054
Registries
EUDAMED
FDA recalls
0

Catalogue2,054

Page 36 of 40

Showing 1,751-1,800 of 2,054

EUDAMED certificates3

EUDAMED certificates (3)

ITALCERT SRL 0426 2 certificates

  • 027-00-08-MDR Supplemented

    Quality management system EU MDR

    Issued
    1 Sep 2026
    Expires
    31 Aug 2028
    Reason
    Add device or group
  • 028-00-04-MDR Supplemented

    Technical documentation EU MDR

    Issued
    1 Sep 2026
    Expires
    31 Aug 2028
    Reason
    Add device or group

ISTITUTO SUPERIORE DI SANITA' 0373 1 certificate

  • CVD0015230125 Issued

    Technical documentation EU MDR

    Issued
    9 Jan 2025
    Expires
    21 Sep 2028

What SIFI S.p.A. makes

SIFI S.p.A. manufactures intraocular lenses (IOLs) and surgical kits designed for cataract procedures, including toric and multifocal variants for presbyopia correction. The products are labeled with specific dioptric powers and optical zone sizes, such as ‘Mini Well’ IOLs and associated implantation kits. These devices are intended for implantation during phacoemulsification surgery to restore vision in patients with cataracts or refractive errors.

The company’s portfolio includes Class IIb and Class III medical devices, regulated under EU medical device legislation. These products are registered in the EU’s eudamed database, ensuring traceability and compliance with EU MDR requirements. The manufacturer is based in Italy.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Address
36, Via Ercole Patti, Aci Sant'antonio Catania, Italy
Phone
+390957922111
EUDAMED SRN
IT-MF-000020853