Corneal trephine manual instrument - UK MHRA Medical Device Registration
Corneal trephine manual instrument is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 103823. The device is manufactured by Moria S.A. from France, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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
Corneal trephine manual instrument
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Oct 31, 2024
Relationship Type
Address
49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG
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