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 181854. 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.
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.
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
Address
Floor 3, Building 1, Lane 500, Furonghua Road, Pudong New Area
Shanghai, China
Created Date
Nov 14, 2023
Relationship Type
Address
3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR
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