Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

Peripheral vascular guidewire, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 101166. The device is manufactured by Arrow International LLC from United States, classified as General Medical Device. The authorized representative in the UK is TFX Group Ltd.

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Peripheral vascular guidewire, manual

MHRA Device ID: 101166•Ref: 101166

Device Type

General Medical Device

Devices

Peripheral vascular guidewire, manual

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 12, 2024

Manufacturer Information

Name

Arrow International LLC

Address

3015 Carrington Mill Blvd

Morrisville, North Carolina, United States

Created Date

Apr 20, 2021

Authorized Representative

Name

TFX Group Ltd

Relationship Type

UK Responsible Person

Address

Grosvenor House Horseshoe Crescent

Old Town Beaconsfield, England, United Kingdom

Postcode: HP9 1LJ

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Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

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Peripheral vascular guidewire, manual

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