United Kingdom MHRA device registration 168701

Cardiac/peripheral vascular guidewire, single-use

United Kingdom·General Medical Device·Cerenovus, Inc.·Registered Sep 12, 2023DREGIY

Registration details

Device ID: 168701
Status: DREGIY
Date Registered: Sep 12, 2023

Device classification

Device Type: General Medical Device
Type: Class III

Manufacturer

Name: Cerenovus, Inc.
Address: 6303 Blue Lagoon Drive, Suites 215 & 315
Miami, Florida, United States

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About this record

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 168701. The device is manufactured by Cerenovus, Inc. from United States, classified as General Medical Device.

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