Dura mater sealant - UK MHRA Medical Device Registration
Dura mater sealant is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184636. The device is manufactured by Integra LifeSciences Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Integra Neurosciences Limited.
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
Dura mater sealant
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
May 1, 2024
Address
1100 Campus Road
Princeton, United States
Created Date
Apr 27, 2021
Relationship Type
Address
Regus Rourke House, Office #113 Watermans Business Park The Causeway
Staines, England, United Kingdom
Postcode: TW18 3BA
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