Phacoemulsification/vitrectomy system - UK MHRA Medical Device Registration
Phacoemulsification/vitrectomy system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 94465. The device is manufactured by Alcon Laboratories, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Alcon Eye Care UK Limited.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, 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
Devices
Phacoemulsification/vitrectomy system
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Apr 23, 2024
Address
6201 South Freeway
Fort Worth, United States
Created Date
Apr 27, 2021
Relationship Type
Address
Park View, Riverside Way Watchmoor Park
Camberley, Surrey, United Kingdom
Postcode: GU15 3YL
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