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ROCHE CARDIAC TROP TSENSITIVE TEST

ROCHE CARDIAC TROP TSENSITIVE TEST
ROCHE CARDIAC TROP TSENSITIVE TEST
ROCHE CARDIAC TROP TSENSITIVE TEST
ROCHE CARDIAC TROP TSENSITIVE TEST

ROCHE CARDIAC TROP TSENSITIVE TEST Specification

  • Shelf Life
  • 24 months from manufacturing
  • Display Type
  • Visual (colored line indication)
  • Function
  • Troponin T detection for acute myocardial infarction diagnosis
  • Usage Type
  • Single Use
  • Instruments Type
  • Point of Care Diagnostic
  • Storage Instructions
  • Store at 2C-30C, avoid frost
  • Measurement Range
  • Qualitative detection, not quantitative
  • Features
  • High sensitivity, easy to use, fast results
  • Accuracy
  • >99%
  • Equipment Type
  • Rapid Test Diagnostic Kit
  • Material
  • Plastic and test membrane
  • Condition
  • New
  • Technology
  • Lateral Flow Immunoassay
  • Portable
  • Yes
  • Wall Mounted
  • No
  • Real-Time Operation
  • Yes
  • Noise Level
  • Silent
  • Operating Type
  • Manual
  • Use
  • Detection of cardiac Troponin T in human blood
  • Dimension (L*W*H)
  • Standard strip size
  • Weight
  • Lightweight (approx 10 g per test device)
  • Color
  • White cassette, colorless membrane
  • CE Marked
  • Yes
  • Test Principle
  • Immunochromatographic assay
  • Time To Result
  • As little as 15 minutes
  • Lot Number and Expiry Date
  • Printed on packaging
  • Packaging
  • Individually sealed pouches with desiccant
  • Sample Type
  • Whole blood, serum, or plasma
  • Sensitivity
  • Highly sensitive (detects low levels of cardiac Troponin T)
  • Intended User
  • Healthcare Professionals
 
 

About ROCHE CARDIAC TROP TSENSITIVE TEST

Cardiac troponin T is a muscle structural protein which is released in the event of cell damage (necrosis) to the myocardium. The TROPT Sensitive test is designed for qualitative determination of cardiac troponin T in the blood as an aid for risk stratification of patients with unstable angina pectoris and for diagnosis of myocardial infarction (STsegment elevation myocardial infarction (STEMI) and NonSTsegment elevation myocardial infarction (NSTEMI)) among patients suffering from thoracic pain or who are suspected of experiencing myocardial infarction or acute coronary syndrome in accordance with the redefinition of myocardial infarction by the ESC (European Society of Cardiology) and the ACC (American College of Cardiology)

as well as the guidelines laid down by the ACC and the AHA (American Heart Association).


A negative troponin T result does not rule out myocardial infarction as the release of troponin T from the damaged myocardial cells into the circulating blood occurs with time delays which vary from person to person.

The release kinetics of troponin T after an infarction should therefore be taken into account when interpreting the test results. Troponin T can first be detected in the blood after a time period of 2 to more than 10 hours after the onset of symptoms. This means that a negative troponin T result does not rule out myocardial infarction. Typical or atypical symptoms and a negative Trop T result call for further diagnostic measures to be applied, including more troponin T tests. Due to its release kinetics, troponin T can be detected for up to 14 days after onset of cardiac infarction.



Quick and Reliable Troponin T Diagnosis

Obtain accurate cardiac Troponin T results in just 15 minutes. The ROCHE CARDIAC TROP TSENSITIVE TEST offers healthcare professionals a fast, user-friendly tool for the diagnosis of acute myocardial infarction, delivering critical decision support at the point of care.


Designed for Healthcare Environments

This kit operates with whole blood, serum, or plasma, making it adaptable to various clinical settings. Its compact, single-use format ensures portability and cleanliness, with no requirement for specialized instruments or electricity.


Safe and Easy Operation

With a manual, real-time operation and simple visual line results, the test is easy for healthcare professionals to perform. Each device is individually packaged with clear lot number and expiry date labeling, ensuring safety and traceability.

FAQ's of ROCHE CARDIAC TROP TSENSITIVE TEST:


Q: How is the ROCHE CARDIAC TROP TSENSITIVE TEST performed?

A: The test is performed manually by applying a drop of whole blood, serum, or plasma onto the test membrane. Results are read visually based on the appearance of colored lines, typically within 15 minutes.

Q: What are the main benefits of using this test in a clinical setting?

A: This test offers high sensitivity for Troponin T detection, fast turnaround times, and portability. It provides reliable support for the rapid diagnosis of acute myocardial infarction without the need for specialized instruments.

Q: When should this test be used?

A: It is designed for situations where rapid detection of cardiac Troponin T is needed-such as in emergency rooms, outpatient clinics, and other point-of-care environments to assist in diagnosing acute myocardial infarction.

Q: Where can the test be stored safely?

A: The kits should be stored at temperatures between 2C and 30C, avoiding frost. Each test is individually sealed with a desiccant to maintain product integrity throughout its 24-month shelf life.

Q: What type of sample is required for the test?

A: You can use whole blood, serum, or plasma samples with this diagnostic kit, ensuring flexibility in different healthcare settings.

Q: Is the test quantitative or qualitative?

A: This device is intended for qualitative detection. It reveals the presence or absence of Troponin T but does not provide a numerical measurement.

Q: How accurate is the ROCHE CARDIAC TROP TSENSITIVE TEST?

A: The test delivers over 99% accuracy, ensuring confidence in clinical decision-making for healthcare professionals.

Price 2000 INR/ Piece

  • Minimum Order Quantity
  • 10 Pieces
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