Peripheral angioplasty balloon catheter, basic - UK MHRA Medical Device Registration
Peripheral angioplasty balloon catheter, basic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 173527. The device is manufactured by Medtronic, Inc from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic Limited.
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Device Type
General Medical Device
Devices
Peripheral angioplasty balloon catheter, basic
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Dec 16, 2023
Name
Medtronic, IncAddress
710 Medtronic Parkway
Minneapolis, MN, United States
Created Date
Feb 2, 2021
Relationship Type
Address
Building 9 Croxley Park
Watford, Herts, England, United Kingdom
Postcode: WD18 8WW
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