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 181852. The device is manufactured by Igenesis (Shanghai) Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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Human papillomavirus (HPV) nucleic acid IVD, probe

MHRA Device ID: 181852•Ref: 181852

Device Type

In Vitro Diagnostic Device

Devices

Human papillomavirus (HPV) nucleic acid IVD, probe

Type

IVD General

Date Registered

Nov 15, 2024

Last Updated

Nov 16, 2023

Manufacturer Information

Name

Igenesis (Shanghai) Co., Ltd.

Address

Floor 3, Building 1, Lane 500, Furonghua Road, Pudong New Area

Shanghai, China

Created Date

Nov 14, 2023

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Other Products from Igenesis (Shanghai) Co., Ltd. (10)

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Human papillomavirus (HPV) nucleic acid IVD, probe - 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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