Inherited haemoglobinopathy IVD, reagent - UK MHRA Medical Device Registration
Inherited haemoglobinopathy IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210277. The device is manufactured by Trinity Biotech (Primus Corporation dba Trinity Biotech) from United States, classified as In Vitro Diagnostic Device.
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Device Type
In Vitro Diagnostic Device
Type
Class A
Status
Date Registered
Feb 8, 2025
Address
4231 E. 75th Terrace
Kansas City, Missouri, United States
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Glycated haemoglobin (HbA1c) IVD, calibrator
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Glycated haemoglobin (HbA1c) IVD, reagent
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Inherited haemoglobinopathy IVD, control
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Inherited haemoglobinopathy IVD, reagent
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Glycated haemoglobin (HbA1C) analyser IVD
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Haemoglobin analyser IVD, laboratory
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Inherited haemoglobinopathy IVD, calibrator
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024
Glycated haemoglobin (HbA1c) IVD, control
Type: In Vitro Diagnostic Device
Registered: Nov 26, 2024

