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 175001. The device is manufactured by Delfi Medical Innovations Inc from Canada, classified as General Medical Device. The authorized representative in the UK is International Associates Limited.

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: 175001•Ref: 175001

Device Type

General Medical Device

Devices

Tourniquet cuff, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Sep 3, 2024

Manufacturer Information

Name

Delfi Medical Innovations Inc

Address

106 - 1099 West 8th Avenue

Vancouver, Canada

Created Date

Nov 17, 2021

Authorized Representative

Name

International Associates Limited

Relationship Type

UK Responsible Person

Address

38 Queen Street

Glasgow, Scotland, United Kingdom

Postcode: G1 3DX

DJ Fang

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Other Products from Delfi Medical Innovations Inc (6)

Other Products from Same Authorized Representative (10)

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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