United Kingdom MHRA device registration 191037

Posterior-chamber intraocular lens, pseudophakic, extended-focus

United Kingdom·System or Procedure Pack·SIFI S.p.A.·Registered Nov 26, 2024

Registration details

Device ID: 191037
MHRA Reference Number: 191037
Date Registered: Nov 26, 2024
Last Updated: Oct 31, 2024

Device classification

Device Type: System or Procedure Pack
Devices: Posterior-chamber intraocular lens, pseudophakic, extended-focus
Type: System or Procedure Pack

Manufacturer

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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About this record

Posterior-chamber intraocular lens, pseudophakic, extended-focus is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 191037. The device is manufactured by SIFI S.p.A. from Italy, classified as System or Procedure Pack. 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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