Buffered sample diluent IVD, automated/semi-automated system - UK MHRA Medical Device Registration

Buffered sample diluent IVD, automated/semi-automated system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 133379. The device is manufactured by Shenzhen Lifotronic Technology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is PureUKCA Ltd.

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Buffered sample diluent IVD, automated/semi-automated system

MHRA Device ID: 133379•Ref: 133379

Device Type

In Vitro Diagnostic Device

Devices

Buffered sample diluent IVD, automated/semi-automated system

Type

IVD General

Date Registered

Dec 9, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Shenzhen Lifotronic Technology Co., Ltd.

Address

Unit A, 4th Floor, Building 15, Yijing Estate, No.1008 Songbai Road, Nanshan District

Shenzhen, China

Created Date

Dec 9, 2021

Authorized Representative

Name

PureUKCA Ltd

Relationship Type

UK Responsible Person

Address

59 St. Martin's Lane

London, Middlesex, England, United Kingdom

Postcode: WC2N 4JS

DJ Fang

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Buffered sample diluent IVD, automated/semi-automated system - UK MHRA Medical Device Registration

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Devices

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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