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 126178. The device is manufactured by Stryker Instruments, a division of Stryker Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Stryker 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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General Medical Device

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Tourniquet cuff, single-use

MHRA Device ID: 126178•Ref: 126178

Device Type

General Medical Device

Devices

Tourniquet cuff, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 7, 2023

Manufacturer Information

Name

Stryker Instruments, a division of Stryker Corporation

Address

4100 E. Milham Ave

Kalamazoo, Michigan, United States

Created Date

Mar 3, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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Other Products from Stryker Instruments, a division of Stryker Corporation (10)

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

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Date Registered

Last Updated

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Created Date

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