United Kingdom MHRA device registration 209386

Posterior-chamber intraocular lens, pseudophakic

United Kingdom·General Medical Device·Alcon Laboratories, Inc.·Registered Jan 23, 2025DREGIY

Registration details

Device ID: 209386
Status: DREGIY
Date Registered: Jan 23, 2025

Device classification

Device Type: General Medical Device
Type: Class IIb

Manufacturer

Name: Alcon Laboratories, Inc.
Address: 6201 South Freeway
Fort Worth, United States

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About this record

Posterior-chamber intraocular lens, pseudophakic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209386. The device is manufactured by Alcon Laboratories, Inc. from United States, classified as General Medical Device.

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