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Global Healthcare Medical
GHM cTnT US Test Kit (FIA) – Quantitative Cardiac Troponin T Testing with 15-Minute Results, High Myocardial Specificity, and Whole Blood/Serum/Plasma Compatibility
GHM cTnT US Test Kit (FIA) – Quantitative Cardiac Troponin T Testing with 15-Minute Results, High Myocardial Specificity, and Whole Blood/Serum/Plasma Compatibility
SKU: GHM cTnT US
Brand: Global Healthcare Medical
Product Overview
Global Healthcare Medical GHM cTnT US Test Kit (FIA) is a fluorescence immunoassay (FIA) designed for the quantitative determination of Cardiac Troponin T (cTnT) in human whole blood, serum, or plasma samples. The kit is intended for use with compatible POCT Analyzers, providing healthcare professionals with a reliable tool for the assessment of myocardial injury.
Cardiac troponin T (cTnT) has high myocardial specificity and sensitivity, making it one of the most ideal markers for the assessment of myocardial infarction. Following myocardial injury, cTnT is released into the bloodstream and can be detected within a few hours, with elevated levels persisting for an extended period. This extended release kinetics provides a valuable diagnostic window for the assessment of patients presenting with suspected acute coronary syndrome.
The GHM cTnT US Test Kit delivers quantitative results in just 15 minutes, with a measuring range of 0.1–10 ng/mL, supporting efficient clinical decision-making in emergency and point-of-care settings.
The kit is intended for in vitro diagnostic use and professional use only, suitable for application scenarios including emergency departments, intensive care units, clinical laboratories, and point-of-care environments. The product line is manufactured under an EN ISO 13485 certified quality management system covering in vitro diagnostic test kits and analyzers used in the detection of cardiac markers based on fluorescence immunochromatography.
Key Features & Benefits
Fluorescence Immunoassay Technology – High-Sensitivity Quantitative Detection
The GHM cTnT US Test Kit is based on fluorescence immunoassay technology, utilizing a sandwich immunodetection method. Fluorescence-labeled detector antibodies bind to the target protein (cTnT) in the sample. The test device contains a membrane coated with cTnT-specific monoclonal antibodies, enabling reliable and consistent quantitative detection.
| Feature | Benefit |
|---|---|
| Fluorescence immunoassay (FIA) | High-sensitivity quantitative detection |
| Sandwich immunodetection method | Reliable and consistent signal generation |
| cTnT-specific monoclonal antibodies | Targeted and accurate measurement |
| Quantitative determination | Precise cTnT concentration results |
High Myocardial Specificity – Ideal Marker for Myocardial Injury Assessment
Cardiac troponin T (cTnT) has high myocardial specificity and sensitivity, making it one of the most ideal markers of myocardial infarction. The high specificity of cTnT helps distinguish cardiac injury from skeletal muscle damage, supporting accurate clinical assessment.
| Feature | Benefit |
|---|---|
| High myocardial specificity | Distinguishes cardiac injury from skeletal muscle damage |
| High sensitivity | Detects small amounts of myocardial injury |
| Extended diagnostic window | Elevated levels persist for extended period after onset |
| Ideal cardiac marker | Supports assessment of myocardial infarction |
Fast Results – 15 Minutes
The GHM cTnT US Test Kit provides quantitative results in just 15 minutes, supporting rapid clinical decision-making and efficient patient workflow in emergency and point-of-care settings.
| Feature | Benefit |
|---|---|
| 15-minute test time | Rapid turnaround for timely clinical decisions |
| Point-of-care compatibility | Suitable for emergency departments, ICUs, and clinical laboratories |
| Efficient workflow | Enables immediate patient assessment |
Wide Measuring Range – 0.1–10 ng/mL
The GHM cTnT US Test Kit supports a broad measuring range of 0.1–10 ng/mL, accommodating a wide variety of cTnT concentrations for comprehensive cardiac marker assessment.
| Parameter | Specification |
|---|---|
| Measuring Range | 0.1–10 ng/mL |
| Specimen | Whole blood (fingerstick or venous) / Serum / Plasma |
| Test Time | 15 minutes |
| Operating Temperature | 18–25°C |
| Storage Temperature | 2–30°C |
Flexible Sample Compatibility – Whole Blood, Serum, and Plasma
The GHM cTnT US Test Kit is compatible with whole blood samples obtained from fingerstick or venous collection, as well as serum and plasma samples, providing flexibility for different clinical workflows and patient sample collection preferences.
| Feature | Benefit |
|---|---|
| Fingerstick whole blood | Convenient point-of-care sample collection |
| Venous whole blood | Standard laboratory sample compatibility |
| Serum samples | Standard laboratory sample compatibility |
| Plasma samples | Alternative sample type for flexible workflows |
| Flexible sample collection | Adaptable to different clinical settings |
ISO 13485 Certified – Quality and Safety Compliance
The product line is manufactured under an EN ISO 13485 certified quality management system, demonstrating compliance with stringent international standards for the design, development, manufacture, and distribution of in vitro diagnostic test kits and analyzers.
| Feature | Benefit |
|---|---|
| EN ISO 13485 certification | Quality management system compliance |
| Cardiac marker scope | Certified for IVD test kits detecting cardiac markers |
| Quality assurance | Meets high standards of quality and safety |
| Professional-grade | Designed for healthcare professional use |
Product Specifications
| Specification | Detail |
|---|---|
| Model / SKU | GHM cTnT US |
| Product Type | Cardiac Troponin T Test Kit (FIA) |
| Catalog Number | VID60-03-011 |
| Intended Use | Quantitative determination of Cardiac Troponin T (cTnT) in human whole blood, serum, or plasma |
| Detection Principle | Fluorescence immunoassay (FIA); sandwich immunodetection |
| Specimen | Whole blood (fingerstick or venous) / Serum / Plasma |
| Test Time | 15 minutes |
| Measuring Range | 0.1–10 ng/mL |
| Operating Temperature | 18–25°C |
| Storage Temperature | 2–30°C |
| Application Scenario | Emergency department, ICU, clinical laboratory, point-of-care |
| Compatible Analyzers | POCT Analyzers (VIM series) |
| Regulatory Status | Manufactured under EN ISO 13485 certified quality management system |
| Intended User | Professional healthcare use only |
| Package Options | 25 tests/kit |
Why Clinical Professionals Choose Global Healthcare Medical
| Consideration | GHM cTnT US |
|---|---|
| Fluorescence immunoassay technology | High-sensitivity quantitative detection |
| High myocardial specificity | Ideal marker for myocardial infarction assessment |
| 15-minute test time | Rapid turnaround for timely decisions |
| Wide measuring range | 0.1–10 ng/mL for comprehensive cTnT monitoring |
| Flexible sample types | Whole blood, serum, or plasma compatibility |
| ISO 13485 certified | Quality management system compliance |
| Point-of-care compatible | Suitable for emergency departments, ICUs, and clinical laboratories |
| Reliable cardiac marker | cTnT supports assessment of myocardial injury and infarction |
About Global Healthcare Medical
Global Healthcare Medical is dedicated to connecting healthcare providers, retailers, and distributors with high-quality medical devices designed for reliable performance. The GHM cTnT US is part of our professional diagnostic line, developed to support accurate, efficient, and connected point-of-care testing in clinical environments.
Our focus is on dependable performance, clear documentation, and responsive support for professional healthcare settings.
