Eyelid speculum, single-use - UK MHRA Medical Device Registration
Eyelid speculum, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 87194. The device is manufactured by Bausch & Lomb GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Bausch & Lomb U.K. 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
Eyelid speculum, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 26, 2024
Relationship Type
Address
106-114 London Road
Kingston upon Thames, Surrey, England, United Kingdom
Postcode: KT2 6TN
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