Eye spud/needle - UK MHRA Medical Device Registration
Eye spud/needle is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 114641. 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..
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Device Type
General Medical Device
Devices
Eye spud/needle
Type
Class I
Date Registered
Jul 2, 2021
Last Updated
Jan 4, 2024
Relationship Type
Address
106-114 London Road
Kingston upon Thames, Surrey, England, United Kingdom
Postcode: KT2 6TN
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