Peripheral angioplasty balloon catheter, drug-coated - UK MHRA Medical Device Registration
Peripheral angioplasty balloon catheter, drug-coated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 213700. The device is manufactured by Bard Peripheral Vascular, Inc. from United States, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class III
Status
Date Registered
Mar 20, 2025
Address
1625 West 3rd Street
Tempe, Arizona, United States
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