We've updated our Privacy Policy to make it clearer how we use your personal data. We use cookies to provide you with a better experience. You can read our Cookie Policy here.

Advertisement

Trinity Biotech Gains European Approval for the Meritas® Troponin I POC Test

Listen with
Speechify
0:00
Register for free to listen to this article
Thank you. Listen to this article using the player above.

Want to listen to this article for FREE?

Complete the form below to unlock access to ALL audio articles.

Read time: Less than a minute

Trinity Biotech has announced that its landmark, high sensitivity Meritas® Troponin I (TnI) point-of-care (POC) test has obtained CE marking, making it the only POC product capable of meeting all the guidelines stipulated by the world’s leading cardiac organizations for the detection of heart attacks.

With CE marking achieved, the Company now intends to release the product for sale in Europe and other carefully selected markets through its specialist Cardiology Distributor network and direct selling teams.

Designed for use with the revolutionary, Meritas POC Analyzer, the Meritas Troponin I test enables fast, accurate triage and intervention for patients presenting at the emergency department with a possible myocardial infarction (MI).

Results, which are traceable to NIST SRM 2921, are comparable to those obtained using traditional top performing laboratory analyzers, and are available in just 15 minutes.

Turnaround times, patient care and outcomes are improved, helping to maximize the use of precious hospital resources and generate significant cost savings. Additional assays are currently being developed to extend the test menu further.