Posterior-chamber intraocular lens, pseudophakic - UK MHRA Medical Device Registration

Posterior-chamber intraocular lens, pseudophakic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 74125. The device is manufactured by SIFI S.p.A. from Italy, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, Ltd. .

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Posterior-chamber intraocular lens, pseudophakic

MHRA Device ID: 74125•Ref: 74125

Device Type

General Medical Device

Devices

Posterior-chamber intraocular lens, pseudophakic

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

SIFI S.p.A.

Address

Via Ercole Patti, 36

Aci S. Antonio, Catania, Italy

Created Date

Apr 20, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Other Products from SIFI S.p.A. (10)

Other Products from Same Authorized Representative (10)

Posterior-chamber intraocular lens, pseudophakic - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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