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 166347. The device is manufactured by AcuFocus, Inc. from United States, classified as System or Procedure Pack. The authorized representative in the UK is Bausch & Lomb U.K. Ltd..

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Posterior-chamber intraocular lens, pseudophakic, extended-focus

MHRA Device ID: 166347•Ref: 166347

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

Dec 6, 2023

Manufacturer Information

Name

AcuFocus, Inc.

Address

32 Discovery Suite 200

Irvine, CA, United States

Created Date

Feb 13, 2023

Authorized Representative

Name

Bausch & Lomb U.K. Ltd.

Relationship Type

UK Responsible Person

Address

106-114 London Road

Kingston upon Thames, Surrey, England, United Kingdom

Postcode: KT2 6TN

DJ Fang

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

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