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

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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Posterior-chamber intraocular lens, pseudophakic, extended-focus

MHRA Device ID: 191037•Ref: 191037

Device Type

System or Procedure Pack

Devices

Posterior-chamber intraocular lens, pseudophakic, extended-focus

Type

System or Procedure Pack

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

DJ Fang

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

Other Products from Same Authorized Representative (10)

Posterior-chamber intraocular lens, pseudophakic, extended-focus - 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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Posterior-chamber intraocular lens, pseudophakic

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Posterior-chamber intraocular lens, pseudophakic

Posterior-chamber intraocular lens, pseudophakic, extended-focus

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