Open-surgery ligator guide sheath - UK MHRA Medical Device Registration
Open-surgery ligator guide sheath is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 79726. The device is manufactured by SentreHEART from United States, classified as General Medical Device. The authorized representative in the UK is AtriCure UK 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
Open-surgery ligator guide sheath
Type
Class IIa
Date Registered
Apr 1, 2021
Last Updated
Nov 23, 2023
Name
SentreHEARTAddress
300 Saginaw Drive
Redwood City, California, United States
Created Date
Apr 1, 2021
Relationship Type
Address
1 Princeton Mews 167-169 London Road
Kingston Upon Thames , Surrey, England, United Kingdom
Postcode: KT2 6PT
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