Implantable sleep apnoea treatment system pulse generator - UK MHRA Medical Device Registration
Implantable sleep apnoea treatment system pulse generator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 112770. The device is manufactured by Nyxoah SA from Belgium, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Obelis UK Ltd.
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
Implantable sleep apnoea treatment system pulse generator
Type
Active implantable Medical device
Date Registered
Nov 12, 2021
Last Updated
Dec 22, 2022
Name
Obelis UK LtdRelationship Type
Address
Sandford Gate, East Point Business Park
Oxford , England, United Kingdom
Postcode: OX4 6LB
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Type: Active implantable device (Directive 90/385/EEC only)
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Type: Active implantable device (Directive 90/385/EEC only)
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Type: Active implantable device (Directive 90/385/EEC only)
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Type: Active implantable device (Directive 90/385/EEC only)
Manufacturer: Nyxoah SA
Implantable sleep apnoea treatment system, fixed-rate
Type: General Medical Device
Registered: Feb 17, 2024
Implantable sleep apnoea treatment system, fixed-rate
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Nov 12, 2021
Medical device adhesive
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Nov 12, 2021
Implantable sleep apnoea treatment system programmer/charger
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Nov 12, 2021
Implantable sleep apnoea treatment system programmer/charger
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Nov 12, 2021
Noninvasive device battery charger
Type: Active implantable device (Directive 90/385/EEC only)
Registered: Nov 12, 2021
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