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 209764. The device is manufactured by Abbott Medical from United States, classified as General Medical Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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General Medical Device

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 209764

Device Type

General Medical Device

Type

Class III

Status

DREGIY

Date Registered

Jan 30, 2025

Manufacturer Information

Name

Abbott Medical

Address

15900 Valley View Court

Sylmar, California, 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

Address

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