Vitreous/aqueous humour replacement medium, intraoperative - UK MHRA Medical Device Registration
Vitreous/aqueous humour replacement medium, intraoperative is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95935. The device is manufactured by OASIS Medical, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience 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
Vitreous/aqueous humour replacement medium, intraoperative
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jan 29, 2024
Address
510-528 S. Vermont Avenue
Glendora, United States
Created Date
Apr 27, 2021
Relationship Type
Address
Aviation Business Park Enterprise Close
Christchurch, England, United Kingdom
Postcode: BH23 6NX
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