Androstenedione IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

Androstenedione IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122648. The device is manufactured by DiaSorin Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is DiaSorin Italia S.p.A. UK Branch.

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Androstenedione IVD, kit, chemiluminescent immunoassay

MHRA Device ID: 122648•Ref: 122648

Device Type

In Vitro Diagnostic Device

Devices

Androstenedione IVD, kit, chemiluminescent immunoassay

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 7, 2024

Manufacturer Information

Name

DiaSorin Inc.

Address

1951 Northwestern Avenue

Stillwater, MN, United States

Created Date

Dec 16, 2021

Authorized Representative

Name

DiaSorin Italia S.p.A. UK Branch

Relationship Type

UK Responsible Person

Address

Central Road

Dartford, England, United Kingdom

Postcode: DA1 5LR

DJ Fang

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Androstenedione IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

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