Influenza A/B virus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Influenza A/B virus 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 195724. 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.

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In Vitro Diagnostic Device

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Influenza A/B virus antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 195724•Ref: 195724

Device Type

In Vitro Diagnostic Device

Devices

Influenza A/B virus 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

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Influenza A/B virus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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Created Date

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DJ Fang

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