Human chorionic gonadotropin beta-core fragment IVD, control - UK MHRA Medical Device Registration
Human chorionic gonadotropin beta-core fragment IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 128619. The device is manufactured by Biochemical Diagnostics, Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Advena 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
Human chorionic gonadotropin beta-core fragment IVD, control
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Dec 20, 2023
Address
180 Heartland Blvd.
Edgewood, New York, United States
Created Date
Dec 27, 2021
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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