Cochlear implant/auditory brainstem implant sound processor - UK MHRA Medical Device Registration
Cochlear implant/auditory brainstem implant sound processor is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 71284. The device is manufactured by Oticon Medical (Neurelec) from France, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Oticon 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
Active implantable device (Directive 90/385/EEC only)
Devices
Cochlear implant/auditory brainstem implant sound processor
Type
Active implantable Medical device
Date Registered
Mar 30, 2021
Last Updated
Dec 22, 2022
Address
Oticon Medical / Neurelec 2720 chemin de Saint-Bernard 2720 chemin de Saint-Bernard
Vallauris, France
Created Date
Mar 30, 2021
Name
Oticon LimitedRelationship Type
Address
Cadzow Industrial Estate
Hamilton, Lanarkshire, United Kingdom
Postcode: ML3 7QE
Cochlear implant/auditory brainstem implant sound processor
Type: General Medical Device
Manufacturer: MED-EL Elektromedizinische Geraete Gesellschaft m.b.H.
Cochlear implant/auditory brainstem implant sound processor
Type: General Medical Device
Manufacturer: Cochlear Ltd
Cochlear implant/auditory brainstem implant sound processor
Type: Active Implantable Device
Manufacturer: MED-EL Elektromedizinische Geraete Gesellschaft m.b.H.
Cochlear implant/auditory brainstem implant sound processor
Type: Active Implantable Device
Manufacturer: Cochlear Ltd
Cochlear implant/auditory brainstem implant sound processor
Type: General Medical Device
Manufacturer: Cochlear Ltd
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Type: Active implantable device (Directive 90/385/EEC only)
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Manufacturer: Stimwave Technologies Incorporated
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Type: Active implantable device (Directive 90/385/EEC only)
Registered: Mar 30, 2021
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Registered: Mar 30, 2021
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Type: Active implantable device (Directive 90/385/EEC only)
Registered: Mar 30, 2021
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