Lacrimal procedural cannula - UK MHRA Medical Device Registration
Lacrimal procedural cannula is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 170137. The device is manufactured by PSI/EYE-KO, Inc. dba Anodyne Surgical 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
Lacrimal procedural cannula
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Nov 22, 2024
Address
804 Corporate Centre Drive
O'Fallon, Missouri, United States
Created Date
Jan 10, 2022
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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