United Kingdom MHRA device registration 213700

Peripheral angioplasty balloon catheter, drug-coated

United Kingdom flagUnited Kingdom·General Medical Device·Bard Peripheral Vascular, Inc.·Registered Mar 20, 2025DREGIY
Registration details
Device ID
213700
Status
DREGIY
Date Registered
Mar 20, 2025
Device classification
Device Type
General Medical Device
Type
Class III
Manufacturer
Address
1625 West 3rd Street
Tempe, Arizona, United States
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About this record

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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