Vascular guide-catheter, single-use - UK MHRA Medical Device Registration

Vascular guide-catheter, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181691. The device is manufactured by Cerenovus, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Vascular guide-catheter, single-use

MHRA Device ID: 181691•Ref: 181691

Device Type

General Medical Device

Devices

Vascular guide-catheter, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

May 15, 2024

Manufacturer Information

Name

Cerenovus, Inc.

Address

6303 Waterford District Drive Suites 215 & 315

Miami, United States

Created Date

May 25, 2023

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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Other Products from Cerenovus, Inc. (10)

Other Products from Same Authorized Representative (10)

Vascular guide-catheter, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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