Patient health record information system application software - UK MHRA Medical Device Registration
Patient health record information system application software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 172370. The device is manufactured by Lenus Health Ltd from Scotland, United Kingdom, classified as General Medical Device.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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
Patient health record information system application software
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Jul 7, 2023
Name
Lenus Health LtdAddress
43 Constitution Street
Edinburgh, Mid Lothian, Scotland, United Kingdom
Created Date
Aug 4, 2022
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Patient health record information system application software
Type: General Medical Device
Registered: Nov 26, 2024
Vulnerable patient home-monitoring software, professional-only
Type: General Medical Device
Registered: Nov 26, 2024
Vulnerable patient home-monitoring software, professional-only
Type: General Medical Device
Registered: Nov 26, 2024
Vulnerable patient home-monitoring software, professional-only
Type: General Medical Device
Registered: Nov 26, 2024

