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 209434. The device is manufactured by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation 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: 209434

Device Type

General Medical Device

Type

Class III

Status

DREGIY

Date Registered

Jan 24, 2025

Manufacturer Information

Name

Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation

Address

4100 Hamline Avenue North

St. Paul, Minnesota, United States

DJ Fang

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Other Products from Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation (10)

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

Device Type

Type

Status

Date Registered

Name

Address

DJ Fang

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