Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration
Cardiac/peripheral vascular guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 164356. The device is manufactured by Cerenovus, Inc. from United States, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class III
Status
Date Registered
May 17, 2023
Name
Cerenovus, Inc.Address
6303 Blue Lagoon Drive, Suites 215 & 315
Miami, Florida, United States
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