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 193366. The device is manufactured by Terumo Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Terumo UK Ltd.

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 193366•Ref: 193366

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Oct 2, 2024

Manufacturer Information

Name

Terumo Corporation

Address

44-1, 2-chome, Hatagaya, Shibuya-ku

Tokyo, Japan

Created Date

Apr 29, 2021

Authorized Representative

Name

Terumo UK Ltd

Relationship Type

UK Responsible Person

Address

Otium House 2 Freemantle Road

Bagshot, Surrey, England, United Kingdom

Postcode: GU19 5LL

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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