Epiretinal/inner limiting membrane scraper, single-use - UK MHRA Medical Device Registration
Epiretinal/inner limiting membrane scraper, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 90992. The device is manufactured by Peregrine Surgical, LLC from United States, classified as General Medical Device. The authorized representative in the UK is Advena 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
Epiretinal/inner limiting membrane scraper, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 12, 2024
Address
51 Britain Drive
New Britain, Pennsylvania, United States
Created Date
Jul 29, 2021
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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