Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical - UK MHRA Medical Device Registration

Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 124782. The device is manufactured by IMMY, 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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Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical

MHRA Device ID: 124782•Ref: 124782

Device Type

In Vitro Diagnostic Device

Devices

Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 7, 2024

Manufacturer Information

Name

IMMY, Inc.

Address

2701 Corporate Centre Dr.

Norman, OK, United States

Created Date

Dec 20, 2021

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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Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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