Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 168036. 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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Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 168036•Ref: 168036

Device Type

In Vitro Diagnostic Device

Devices

Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA)

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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Multiple Aspergillus species antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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Last Updated

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Created Date

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Address

DJ Fang

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