Human papillomavirus (HPV) nucleic acid IVD, control - UK MHRA Medical Device Registration

Human papillomavirus (HPV) nucleic acid IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 131270. The device is manufactured by LGC Clinical Diagnostics, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is QCS International LTD..

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Human papillomavirus (HPV) nucleic acid IVD, control

MHRA Device ID: 131270•Ref: 131270

Device Type

In Vitro Diagnostic Device

Devices

Human papillomavirus (HPV) nucleic acid IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

LGC Clinical Diagnostics, Inc.

Address

37 Birch Street

Milford, Massachusetts, United States

Created Date

Apr 30, 2021

Authorized Representative

Name

QCS International LTD.

Relationship Type

UK Responsible Person

Address

Suite 9 Cumbernauld Business Park Wardpark Road

Cumbernauld, North Lanarkshire, Scotland, United Kingdom

Postcode: G67 3JZ

DJ Fang

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Human papillomavirus (HPV) nucleic acid IVD, control - 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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