Tourniquet cuff, single-use - UK MHRA Medical Device Registration

Tourniquet cuff, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 98347. The device is manufactured by Terumo Medical Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Terumo UK 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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Tourniquet cuff, single-use

MHRA Device ID: 98347•Ref: 98347

Device Type

General Medical Device

Devices

Tourniquet cuff, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 2, 2024

Manufacturer Information

Name

Terumo Medical Corporation

Address

950 Elkton Boulevard

Elkton, Maryland, United States

Created Date

Aug 25, 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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Tourniquet cuff, single-use - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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