Ureteropelvic balloon catheter - UK MHRA Medical Device Registration

Ureteropelvic balloon catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91826. The device is manufactured by Gyrus ACMI, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is KeyMed (Medical & Industrial Equipment) 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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Ureteropelvic balloon catheter

MHRA Device ID: 91826•Ref: 91826

Device Type

General Medical Device

Devices

Ureteropelvic balloon catheter

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 10, 2024

Manufacturer Information

Name

Gyrus ACMI, Inc.

Address

9600 Louisiana Ave.

North Brooklyn Park, United States

Created Date

Jul 23, 2021

Authorized Representative

Name

KeyMed (Medical & Industrial Equipment) Ltd.

Relationship Type

UK Responsible Person

Address

Keymed House Stock Road

Southend-on-sea, Essex, United Kingdom

Postcode: SS2 5QH

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Ureteropelvic balloon catheter - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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DJ Fang

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