Eye anterior segment analyser - UK MHRA Medical Device Registration
Eye anterior segment analyser is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 131295. The device is manufactured by ArcScan, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP LIMITED.
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Device Type
General Medical Device
Devices
Eye anterior segment analyser
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 10, 2023
Name
ArcScan, Inc.Address
433 Park Point Drive, Suite 220
Golden, CO, United States
Created Date
Jan 6, 2022
Relationship Type
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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