Pulse oximeter - UK MHRA Medical Device Registration
Pulse oximeter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 93154. The device is manufactured by Shenzhen Viatom Technology Co Ltd from China, classified as General Medical Device. The authorized representative in the UK is Medimap 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
General Medical Device
Devices
Pulse oximeter
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Jun 15, 2024
Address
4E Building 3, Tingwei Industrial Park No 6 Liufang Road, Block 67 Xin'an Street Baoan District,
Guangdong, Shenzhen, China
Created Date
Jul 8, 2021
Name
Medimap LtdRelationship Type
Address
2 The Drift
Thurston, Suffolk, United Kingdom
Postcode: IP31 3RT
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