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Nasal cavity stent, removable, prefabricated - UK MHRA Medical Device Registration

Nasal cavity stent, removable, prefabricated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 130066. 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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General Medical Device
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Nasal cavity stent, removable, prefabricated
MHRA Device ID: 130066•Ref: 130066

Device Type

General Medical Device

Devices

Nasal cavity stent, removable, prefabricated

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Nov 13, 2024

Manufacturer Information

Address

Wettersteinstr. 20

Wallgau, Germany

Created Date

Dec 31, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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