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 89863. The device is manufactured by Willy Rusch from Germany, classified as General Medical Device. The authorized representative in the UK is TFX Group Ltd.

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Ureteropelvic balloon catheter

MHRA Device ID: 89863•Ref: 89863

Device Type

General Medical Device

Devices

Ureteropelvic balloon catheter

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Mar 19, 2024

Manufacturer Information

Name

Willy Rusch

Address

Willy Rusch GmbH Willy-Rusch-Strabe 4 71394 Kernen im Remstal Germany

Kernen, Germany

Created Date

Apr 21, 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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Ureteropelvic balloon catheter - UK MHRA Medical Device Registration

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