United Kingdom MHRA device registration 103140

Pulse oximeter

United Kingdom·General Medical Device·TaiDoc Technology Corp·Registered Sep 15, 2024

Registration details

Device ID: 103140
MHRA Reference Number: 103140
Date Registered: Sep 15, 2024
Last Updated: Mar 23, 2024

Device classification

Device Type: General Medical Device
Devices: Pulse oximeter
Type: Class IIb

Manufacturer

Name: TaiDoc Technology Corp
Address: B1-7F, No 127 Wugong 2nd Road
New Taipei City, Wugu Dist, Taiwan
Created Date: Sep 7, 2021

Authorized Representative

Name: Medimap Ltd
Relationship Type: UK Responsible Person
Address: 2 The Drift
Thurston, Suffolk, United Kingdom
Postcode: IP31 3RT

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About this record

Pulse oximeter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 103140. The device is manufactured by TaiDoc Technology Corp from Taiwan, 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.

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