Nasal cavity stent, removable, prefabricated
United Kingdom·General Medical Device·Alaxo GmbH·Registered Nov 26, 2024- Device ID
- 130066
- MHRA Reference Number
- 130066
- Date Registered
- Nov 26, 2024
- Last Updated
- Nov 13, 2024
- Device Type
- General Medical Device
- Devices
- Nasal cavity stent, removable, prefabricated
- Type
- Class I
- Name
- Alaxo GmbH
- Address
- Wettersteinstr. 20 Wallgau, Germany
- Created Date
- Dec 31, 2021
- Relationship Type
- UK Responsible Person
- Address
- 6 Wilmslow Road, Rusholme Manchester, England, United KingdomPostcode: M14 5TP
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by MDSS-UK RP LIMITED in the UK
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.