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United Kingdom MHRA device registration 210276

Glycated haemoglobin (HbA1c) IVD, reagent

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Trinity Biotech (Primus Corporation dba Trinity Biotech)·Registered Feb 8, 2025DREGIY
Registration details
Device ID
210276
Status
DREGIY
Date Registered
Feb 8, 2025
Device classification
Device Type
In Vitro Diagnostic Device
Type
Class A
Manufacturer
Name
Trinity Biotech (Primus Corporation dba Trinity Biotech)
Address
4231 E. 75th Terrace
Kansas City, Missouri, United States
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About this record

Glycated haemoglobin (HbA1c) IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210276. The device is manufactured by Trinity Biotech (Primus Corporation dba Trinity Biotech) from United States, classified as In Vitro Diagnostic Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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