Luteinizing hormone (LH) IVD, reagent - UK MHRA Medical Device Registration
Luteinizing hormone (LH) IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 128055. The device is manufactured by Tosoh Corporation from Japan, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Tosoh Bioscience Limited.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
In Vitro Diagnostic Device
Devices
Luteinizing hormone (LH) IVD, reagent
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
May 3, 2024
Relationship Type
Address
Lytchett House Wareham Road 13 Freeland Park
Poole, Dorset, England, United Kingdom
Postcode: BH16 6FA
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Type: In Vitro Diagnostic Device
Manufacturer: Tosoh Corporation
Adrenocorticotropic hormone (ACTH) IVD, calibrator
Type: In Vitro Diagnostic Device
Manufacturer: Tosoh Corporation
Adrenocorticotropic hormone (ACTH) IVD, kit, enzyme immunoassay (EIA)
Type: In Vitro Diagnostic Device
Manufacturer: Tosoh Corporation
Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA)
Type: In Vitro Diagnostic Device
Manufacturer: Tosoh Corporation
Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent
Type: In Vitro Diagnostic Device
Manufacturer: Tosoh Corporation
B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, calibrator
Type: In Vitro Diagnostic Device
Manufacturer: Tosoh Corporation
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Type: In Vitro Diagnostic Device
Manufacturer: Tosoh Corporation
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Manufacturer: Tosoh Corporation

