Sleep-disordered breathing nasopharyngeal stent, reusable - UK MHRA Medical Device Registration

Sleep-disordered breathing nasopharyngeal stent, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 130065. The device is manufactured by Alaxo GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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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Sleep-disordered breathing nasopharyngeal stent, reusable

MHRA Device ID: 130065•Ref: 130065

Device Type

General Medical Device

Devices

Sleep-disordered breathing nasopharyngeal stent, reusable

Type

Class I

Date Registered

Dec 31, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Alaxo GmbH

Address

Frickenstr. 5

Krün, Germany

Created Date

Dec 31, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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Type: General Medical Device

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Sleep-disordered breathing nasopharyngeal stent, reusable - UK MHRA Medical Device Registration

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