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.

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Pulse oximeter

MHRA Device ID: 93154•Ref: 93154

Device Type

General Medical Device

Devices

Pulse oximeter

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 15, 2024

Manufacturer Information

Name

Shenzhen Viatom Technology Co Ltd

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

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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