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 95175. The device is manufactured by NIDEK CO., LTD. from Japan, classified as General Medical Device. The authorized representative in the UK is Advena Ltd.
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 13, 2024
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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