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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 94736. The device is manufactured by Elekta Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Elekta 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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General Medical Device
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Patient health record information system application software
MHRA Device ID: 94736•Ref: 94736

Device Type

General Medical Device

Devices

Patient health record information system application software

Type

Class IIb

Date Registered

Aug 13, 2021

Last Updated

Oct 13, 2022

Manufacturer Information

Address

100 Mathilda Place Fifth Floor

Sunnyvale, California, United States

Created Date

Aug 13, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Cornerstone London Road

Crawley, West Sussex, United Kingdom

Postcode: RH10 9BL

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