United Kingdom MHRA device registration 81589

Sleep disorder interpretive software, patient-use

United Kingdom flagUnited Kingdom·General Medical Device·ResApp Health Limited·Registered May 20, 2021
Registration details
Device ID
81589
MHRA Reference Number
81589
Date Registered
May 20, 2021
Last Updated
Dec 7, 2023
Device classification
Device Type
General Medical Device
Devices
Sleep disorder interpretive software, patient-use
Type
Class I
Manufacturer
Address
138 Juliette Street Greenslopes
Brisbane , Queensland, Australia
Created Date
May 20, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP
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About this record

Sleep disorder interpretive software, patient-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 81589. The device is manufactured by ResApp Health Limited from Australia, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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.

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