Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing - UK MHRA Medical Device Registration
Luteinizing hormone (LH) IVD, kit, rapid ICT, self-testing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178929. The device is manufactured by Sugentech, Inc. from South Korea, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting Ltd.
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, kit, rapid ICT, self-testing
Type
IVD Devices for Self-Testing
Date Registered
Nov 26, 2024
Last Updated
Oct 22, 2024
Name
Sugentech, Inc.Address
721-26, Jeongjungyeonje-ro, Osong-eup, Heungdeok-gu
Cheongju-si, Chungcheongbuk-do, South Korea
Created Date
Jun 29, 2021
Relationship Type
Address
Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP
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