Posterior-chamber intraocular lens, pseudophakic - UK MHRA Medical Device Registration
Posterior-chamber intraocular lens, pseudophakic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 207606. The device is manufactured by Bausch & Lomb Incorporated from United States, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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.
Device Type
General Medical Device
Type
Class IIb
Status
Date Registered
Dec 21, 2024
Address
1400 North Goodman Street
Rochester, New York, United States
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Posterior-chamber intraocular lens, pseudophakic
Type: General Medical Device
Registered: Dec 21, 2024
Posterior-chamber intraocular lens, pseudophakic
Type: General Medical Device
Registered: Dec 21, 2024
Posterior-chamber intraocular lens, pseudophakic
Type: General Medical Device
Registered: Dec 21, 2024
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