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

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General Medical Device

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 168701

Device Type

General Medical Device

Type

Class III

Status

DREGIY

Date Registered

Sep 12, 2023

Manufacturer Information

Name

Cerenovus, Inc.

Address

6303 Blue Lagoon Drive, Suites 215 & 315

Miami, Florida, United States

DJ Fang

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Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

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Date Registered

Name

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Cardiac/peripheral vascular guidewire, single-use