United Kingdom MHRA device registration 150654

Total human chorionic gonadotropin (HCG) IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·VicTorch Meditek, Inc.·Registered Jun 30, 2022

Registration details

Device ID: 150654
MHRA Reference Number: 150654
Date Registered: Jun 30, 2022
Last Updated: Apr 13, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Total human chorionic gonadotropin (HCG) IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: VicTorch Meditek, Inc.
Address: 6888 Nancy Ridge Drive
San Diego, California, United States
Created Date: Jun 30, 2022

Authorized Representative

Name: UKCApartner4U Limited
Relationship Type: UK Responsible Person
Address: 7 CAMPION WAY
BINGHAM, NOTTINGHAM, England, United Kingdom
Postcode: NG13 8 TR

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About this record

Total human chorionic gonadotropin (HCG) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 150654. The device is manufactured by VicTorch Meditek, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U 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.

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