Air-conduction hearing aid, in-the-ear - UK MHRA Medical Device Registration
Air-conduction hearing aid, in-the-ear is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92367. The device is manufactured by Sonova AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is Sonova UK 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.
Device Type
General Medical Device
Devices
Air-conduction hearing aid, in-the-ear
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
May 17, 2024
Name
Sonova AGAddress
Sonova AG Laubisruetistrasse 28
Staefa, Zurich, Switzerland
Created Date
Aug 4, 2021
Relationship Type
Address
Sonova House Lakeside Drive Centre Park Square
Warrington, England, United Kingdom
Postcode: WA1 1RX
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Type: General Medical Device
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Type: General Medical Device
Manufacturer: Phonak AG
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Type: General Medical Device
Manufacturer: Sonova AG
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Type: General Medical Device
Manufacturer: Sonova AG
Audiometric/hearing device software
Type: General Medical Device
Manufacturer: Sonova AG
Air-conduction hearing aid fitting kit
Type: General Medical Device
Manufacturer: Sonova AG
Air-conduction hearing aid, canal
Type: General Medical Device
Manufacturer: Sonova AG
Air-conduction hearing aid, in-the-ear
Type: General Medical Device
Manufacturer: Sonova AG
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Air-conduction hearing aid, behind-the-ear
Type: General Medical Device
Manufacturer: Sonova AG

