Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 192687. The device is manufactured by Biomerica, 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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Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 192687•Ref: 192687

Device Type

In Vitro Diagnostic Device

Devices

Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jan 25, 2024

Manufacturer Information

Name

Biomerica, Inc.

Address

17571 VON KARMAN AVE.

Irvine, CA, United States

Created Date

Apr 17, 2023

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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Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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