SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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 202257. The device is manufactured by CTK Biotech, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP 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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SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 202257•Ref: 202257

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 27, 2024

Manufacturer Information

Name

CTK Biotech, Inc.

Address

13855 Stowe Dr.

Poway, CA, United States

Created Date

Jun 21, 2024

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

MedTech Regulatory Expert

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Other Products from CTK Biotech, Inc. (10)

Other Products from Same Authorized Representative (10)

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