Angiographic catheter, single-use - UK MHRA Medical Device Registration
Angiographic catheter, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205381. The device is manufactured by Cordis US Corp. from United States, classified as General Medical Device. The authorized representative in the UK is Cordis Medical UK Limited.
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Device Type
General Medical Device
Devices
Angiographic catheter, single-use
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Nov 10, 2023
Name
Cordis US Corp.Address
14201 North West 60th Avenue
Miami Lakes, Florida, United States
Created Date
Sep 23, 2022
Relationship Type
Address
Suite 402, Chadwick House Birchwood Park
Warrington, England, United Kingdom
Postcode: WA3 6AE
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Angiographic catheter, single-use
Type: General Medical Device
Manufacturer: Cordis US Corp.

