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 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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Pulse oximeter

MHRA Device ID: 103140•Ref: 103140

Device Type

General Medical Device

Devices

Pulse oximeter

Type

Class IIb

Date Registered

Sep 15, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

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

DJ Fang

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Pulse oximeter - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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