Nasal/paranasal balloon catheter - UK MHRA Medical Device Registration

Nasal/paranasal balloon catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85631. The device is manufactured by Entellus Medical, Inc 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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Nasal/paranasal balloon catheter

MHRA Device ID: 85631•Ref: 85631

Device Type

General Medical Device

Devices

Nasal/paranasal balloon catheter

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 8, 2023

Manufacturer Information

Name

Entellus Medical, Inc

Address

3600 Holly Lane North Suite 40

Plymouth, Minnesota, United States

Created Date

Feb 26, 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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Nasal/paranasal balloon catheter - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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