United Kingdom MHRA device registration 102411

SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·Hangzhou Funworld Biotech. Co., Ltd·Registered Nov 26, 2024

Registration details

Device ID: 102411
MHRA Reference Number: 102411
Date Registered: Nov 26, 2024
Last Updated: Jan 13, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: Hangzhou Funworld Biotech. Co., Ltd
Address: Room 301, Buliding 1#, 136 Zhiyi Rd, Yuhang Sub-district, Yuhang District,
Hangzhou, Zhejiang, China
Created Date: Sep 3, 2021

Authorized Representative

Name: NPZ technology Ltd
Relationship Type: UK Responsible Person
Address: Stirling House Cambridge Innovation Park, Denny End Road, Waterbeach
Cambridge, Cambridgeshire, United Kingdom
Postcode: CB25 9QE

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About this record

SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 102411. The device is manufactured by Hangzhou Funworld Biotech. Co., Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is NPZ technology Ltd.

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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