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

Human papillomavirus (HPV) 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 153638. The device is manufactured by Guangzhou Pluslife Biotech Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Human papillomavirus (HPV) nucleic acid IVD, kit, nucleic acid technique (NAT)
MHRA Device ID: 153638โ€ขRef: 153638

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 8, 2023

Manufacturer Information

Address

Room 402, 6 Lianhuayan Road, Huangpu District, Guangzhou

Guangdong Province, China

Created Date

Aug 5, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

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