SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay, rapid - UK MHRA Medical Device Registration

SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay, rapid is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 153340. The device is manufactured by ACON Biotech (Hangzhou) Co Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap 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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SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay, rapid

MHRA Device ID: 153340•Ref: 153340

Device Type

In Vitro Diagnostic Device

Devices

SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay, rapid

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

Name

ACON Biotech (Hangzhou) Co Ltd

Address

No 210 Zhenzhong Road West Lake District

Hangzhou, China

Created Date

Jan 25, 2021

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

MedTech Regulatory Expert

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Other Products from ACON Biotech (Hangzhou) Co Ltd (10)

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SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay, rapid - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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