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 207605. The device is manufactured by Bausch & Lomb Incorporated from United States, classified as General Medical Device.
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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: System or Procedure Pack
Manufacturer: Caregroup Sight Solution Private Limited
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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