Loupe - UK MHRA Medical Device Registration
Loupe is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210427. The device is manufactured by Leica Microsystems (Schweiz) AG from Switzerland, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Type
Class I
Status
Date Registered
Feb 11, 2025
Address
Max Schmidheiny-Strasse 201
Heerbrugg, Switzerland
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