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

Human papillomavirus (HPV) nucleic acid IVD, probe is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 165425. The device is manufactured by Advanced Cell Diagnostics, Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Human papillomavirus (HPV) nucleic acid IVD, probe

MHRA Device ID: 165425•Ref: 165425

Device Type

In Vitro Diagnostic Device

Devices

Human papillomavirus (HPV) nucleic acid IVD, probe

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

Advanced Cell Diagnostics, Inc

Address

7707 Gateway Blvd.

Newark, California, United States

Created Date

Jan 25, 2023

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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Other Products from Advanced Cell Diagnostics, Inc (1)

Nucleic acid hybridization detection IVD, control

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

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

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Date Registered

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DJ Fang

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