Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid - UK MHRA Medical Device Registration

Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 138165. The device is manufactured by Quidel Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid

MHRA Device ID: 138165•Ref: 138165

Device Type

In Vitro Diagnostic Device

Devices

Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 10, 2023

Manufacturer Information

Name

Quidel Corporation

Address

10165 McKellar Ct.

San Diego CA, United States

Created Date

Feb 25, 2022

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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Human chorionic gonadotropin beta-subunit (beta-HCG) IVD, kit, immunochromatographic test (ICT), rapid - UK MHRA Medical Device Registration

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Created Date

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Address

DJ Fang

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