Peripheral artery endovascular stent-graft, non-medicated - UK MHRA Medical Device Registration
Peripheral artery endovascular stent-graft, non-medicated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 72985. The device is manufactured by Atrium Medical Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Getinge 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
Peripheral artery endovascular stent-graft, non-medicated
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Jul 23, 2024
Address
Continental drive 40
Merimack, United States
Created Date
Apr 13, 2021
Name
Getinge LimitedRelationship Type
Address
Unit 3 St Modwen Park Andressey Way Chaddesden
Derby, England, United Kingdom
Postcode: DE21 6YH
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