United Kingdom MHRA device registration 165425

Human papillomavirus (HPV) nucleic acid IVD, probe

United Kingdom·In Vitro Diagnostic Device·Advanced Cell Diagnostics, Inc·Registered Nov 26, 2024

Registration details

Device ID: 165425
MHRA Reference Number: 165425
Date Registered: Nov 26, 2024
Last Updated: May 9, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Human papillomavirus (HPV) nucleic acid IVD, probe
Type: IVD General

Manufacturer

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

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About this record

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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