The Troponin I Rapid Test Kit (Mono Pack) is a rapid immunochromatographic lateral flow assay designed for the qualitative detection of Cardiac Troponin I (cTnI) in human whole blood, serum, or plasma, according to the manufacturer's instructions. Cardiac Troponin I is a highly specific biomarker released into the bloodstream following injury to heart muscle cells and is widely used by healthcare professionals during the evaluation of patients with suspected Acute Myocardial Infarction (AMI) and other causes of myocardial injury.
Designed for professional in-vitro diagnostic (IVD) use, this single-test (mono pack) format is suitable for hospitals, emergency departments, intensive care units, diagnostic laboratories, physician clinics, ambulances, and other healthcare settings where rapid cardiac assessment is required.
Microsidd supplies genuine diagnostic products with secure packaging, reliable dispatch, and nationwide delivery across India.
Product Name: Troponin I Rapid Test Kit (Mono Pack)
Test Type: Rapid Immunochromatographic Cardiac Marker Test
Biomarker Detected: Cardiac Troponin I (cTnI)
Result Type: Qualitative
Intended Use: Professional In-Vitro Diagnostic (IVD) Use
Sample Type: Human Whole Blood, Serum or Plasma (refer to manufacturer instructions)
Pack Size: Mono Pack (Single Test)
Suitable For: Hospitals, Emergency Departments, ICUs, Diagnostic Laboratories, Clinics and Healthcare Professionals
The Troponin I Rapid Test Kit is a point-of-care diagnostic test that detects Cardiac Troponin I (cTnI), one of the most clinically important biomarkers used in the evaluation of myocardial injury.
When heart muscle cells are damaged, Cardiac Troponin I may be released into the bloodstream. Healthcare professionals commonly use Troponin I testing, together with clinical assessment, ECG findings, patient history, and additional laboratory investigations, when evaluating patients presenting with symptoms such as chest pain or suspected acute coronary syndrome.
This rapid test provides a qualitative result and is intended to support clinical decision-making. It should not be used as the sole basis for diagnosis.
The Troponin I Rapid Test Kit may be used by healthcare professionals for:
Evaluation of patients with suspected Acute Myocardial Infarction (AMI)
Assessment of chest pain in emergency settings
Cardiac biomarker testing
Emergency department triage
Intensive care and coronary care units
Hospital and diagnostic laboratory testing
Physician clinics and medical centres
Point-of-care cardiac assessment
Rapid qualitative detection of Cardiac Troponin I (cTnI)
Designed for professional in-vitro diagnostic use
Single-test mono pack for convenient point-of-care testing
Immunochromatographic lateral flow technology
Easy-to-use testing procedure
Suitable for emergency and critical care settings
Supports timely clinical assessment
Compact format for individual patient testing
Genuine diagnostic product supplied by Microsidd
The Troponin I Rapid Test Kit uses an immunochromatographic lateral flow assay. A patient specimen is applied to the sample well, where Cardiac Troponin I, if present, binds to labeled antibodies within the test device. The resulting immune complexes migrate across the membrane and produce visible test and control lines according to the manufacturer's interpretation guide.
The result is qualitative and should always be interpreted alongside the patient's symptoms, ECG findings, medical history, and other laboratory investigations.
This product is intended for use by:
Cardiologists
Emergency physicians
Critical care specialists
Hospital laboratories
Diagnostic laboratories
Pathologists
Medical colleges
Healthcare institutions
Qualified laboratory personnel
Each mono pack typically contains:
1 Troponin I Rapid Test Device
Sample dropper or transfer device (where supplied)
Buffer reagent (if applicable)
Manufacturer's Instructions for Use (IFU)
Please refer to the product packaging for the exact contents.
Bring the test kit and specimen to the recommended operating temperature.
Collect the patient specimen according to laboratory protocols.
Add the required specimen volume to the sample well.
Add buffer if instructed by the manufacturer.
Allow the test to develop for the recommended time.
Read the result only within the specified interpretation window.
Dispose of all used materials according to biomedical waste regulations.
Always follow the manufacturer's instructions supplied with the kit.
| Feature | Details |
|---|---|
| Product Name | Troponin I Rapid Test Kit |
| Pack Size | Mono Pack (Single Test) |
| Biomarker | Cardiac Troponin I (cTnI) |
| Test Method | Immunochromatographic Lateral Flow Assay |
| Result Type | Qualitative |
| Intended Use | Professional IVD |
| Sample Type | Whole Blood / Serum / Plasma (Refer IFU) |
| Application | Cardiac Marker Testing |
| Usage | Single Use |
| Specification | Details |
|---|---|
| Product Category | Cardiac Marker Rapid Test |
| Detection Target | Cardiac Troponin I (cTnI) |
| Method | Immunochromatographic Assay |
| Result | Qualitative |
| Sample | Whole Blood / Serum / Plasma (Refer IFU) |
| Intended User | Healthcare Professionals |
| Usage | Single Use |
| Storage | As per Manufacturer Instructions |
Store according to the manufacturer's recommended temperature.
Keep the test device in its sealed pouch until use.
Protect from excessive heat, humidity and direct sunlight.
Do not freeze unless specified by the manufacturer.
Do not use beyond the expiry date.
Do not reuse the test device.
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The test qualitatively detects Cardiac Troponin I (cTnI), a biomarker that may become elevated following myocardial injury.
This product is intended for at-home by professional in-vitro diagnostic use only.
Refer to the manufacturer's instructions for approved specimen types, which may include whole blood, serum and plasma.
The Troponin I Rapid Test supports the clinical evaluation of patients with suspected myocardial injury. It should not be used as the sole basis for diagnosis.
No. Clinical decisions should consider symptoms, ECG findings, patient history, timing of symptom onset, repeat testing when appropriate, and other laboratory investigations.
No. This rapid test provides a qualitative result.
Store according to the manufacturer's instructions and do not use after the expiry date.
No. Each test device is intended for single use only.
Hospitals, emergency departments, coronary care units, intensive care units, diagnostic laboratories, physician clinics, and ambulances.
Microsidd supplies genuine diagnostic products with reliable customer support, secure packaging, and nationwide delivery across India.
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The Troponin I Rapid Test Kit (Mono Pack) is an in-vitro diagnostic medical device intended for professional use only. Results should be interpreted by qualified healthcare professionals together with the patient's clinical presentation, medical history, electrocardiogram (ECG), imaging findings, and other laboratory investigations. This product is not intended for self-testing or as the sole basis for diagnosing or excluding myocardial infarction or other cardiac conditions.
The troponin I test is used to measure the levels of troponin I, a protein found in cardiac muscle cells. It is primarily used as a diagnostic tool to assess and monitor heart health, particularly in cases of suspected heart injury or damage.
Troponin I is released into the bloodstream when there is damage to the heart muscle, such as during a heart attack or myocardial infarction (MI). The test detects the presence and levels of troponin I in the blood, which helps in diagnosing and evaluating the severity of a heart attack.
The troponin I test is highly sensitive and specific for detecting heart muscle damage. It is often preferred over other cardiac enzyme tests, such as creatine kinase (CK) or lactate dehydrogenase (LDH), due to its greater specificity for cardiac injury.
Here are some key uses and applications of the troponin I test:
1. Diagnosis of a heart attack: Troponin I levels rise within a few hours after the onset of a heart attack and remain elevated for several days. By measuring troponin I levels, doctors can confirm the diagnosis of a heart attack and determine the extent of damage to the heart muscle.
2. Risk stratification: Troponin I levels can help assess the risk and prognosis of a heart attack. Higher levels of troponin I generally indicate a larger area of heart muscle damage and a worse prognosis.
3. Monitoring cardiac injury: Troponin I levels can be monitored over time to evaluate the progress of cardiac injury, assess the effectiveness of treatment, and determine the need for additional interventions.
4. Detecting other heart conditions: Elevated troponin I levels may indicate other heart-related conditions, such as unstable angina, congestive heart failure, or inflammation of the heart muscle (myocarditis).
It's important to note that troponin I is specific to cardiac muscle, so an elevated troponin I level indicates heart muscle damage rather than damage to other organs.
If you have concerns about your heart health or have experienced symptoms of a heart attack, it's crucial to consult a healthcare professional who can evaluate your symptoms, order appropriate tests like the troponin I test if necessary, and provide appropriate medical advice and treatment.
For the qualitative detection of cardia Tropnin I (cTnl) and its Complexity at a level equal to or higher than 0.25 ng/mL
15 Minutes results
Sensitivity 0.25 ng/mL for serum/plasma, 1 ng/mL for whole blood sample
Specificity 98%
Storage room temperature Refrigerator not required
Contents: 1 Troponin i Test Kit , 1 Lancet, 1 Swab, User Guide.
| Specification name | Specification Value |
|---|---|
| Test method | At-home test (self-administered), Point-of-care test, RDT |
| Test sample | Blood |