Catheter/overtube balloon inflator, single-use - UK MHRA Medical Device Registration

Catheter/overtube balloon inflator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96768. The device is manufactured by Medtronic Sofamor Danek Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic Limited.

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Catheter/overtube balloon inflator, single-use

MHRA Device ID: 96768•Ref: 96768

Device Type

General Medical Device

Devices

Catheter/overtube balloon inflator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 16, 2023

Manufacturer Information

Name

Medtronic Sofamor Danek Inc.

Address

1800 Pyramid Place

Memphis, TN, United States

Created Date

Mar 9, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Catheter/overtube balloon inflator, single-use - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

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Address

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