Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT) - UK MHRA Medical Device Registration

Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 162319. The device is manufactured by PreTect AS from Norway, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MedEnvoy UK Limited.

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In Vitro Diagnostic Device

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Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT)

MHRA Device ID: 162319•Ref: 162319

Device Type

In Vitro Diagnostic Device

Devices

Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 24, 2023

Manufacturer Information

Name

PreTect AS

Address

Ustadhagan 8

Klokkarstua, Norway

Created Date

Dec 7, 2022

Authorized Representative

Name

MedEnvoy UK Limited

Relationship Type

UK Responsible Person

Address

85 Great Portland Street First Floor

London, England, United Kingdom

Postcode: W1W 7LT

DJ Fang

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Human papillomavirus (HPV) high risk strain nucleic acid IVD, kit, nucleic acid technique (NAT) - UK MHRA Medical Device Registration

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