United Kingdom MHRA device registration 207605

Posterior-chamber intraocular lens, pseudophakic

United Kingdom·General Medical Device·Bausch & Lomb Incorporated·Registered Dec 21, 2024DREGIY

Registration details

Device ID: 207605
Status: DREGIY
Date Registered: Dec 21, 2024

Device classification

Device Type: General Medical Device
Type: Class IIb

Manufacturer

Name: Bausch & Lomb Incorporated
Address: 1400 North Goodman Street
Rochester, New York, 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 207605. The device is manufactured by Bausch & Lomb Incorporated from United States, classified as General Medical Device.

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