Clinical Safety and Efficacy Testing of a Medical Device Kardi Ai, an ECG Telemetry Monitoring System
The goal of this clinical trial is to evaluate the safety and efficacy of medical device Kardi Ai, an ECG telemetry monitoring device in adult population.
The main questions it aims to answer are:
* What is the sensitivity and specificity of Kardi Ai device for all monitored heart rythm disorders (combined)
* What is the sensitivity and specificity of Kardi Ai device for each of the monitored heart rythm disorders
* What is the quality of the ECG recordings
Participants will receive Kardi Ai medical device. They will use it to collect ECG recordings from at least 5 different days and in total collect records of at least 10 hours duration.
Gender: All
Ages: 18 Years - Any
Atrial Fibrillation (AF)
Atrial Premature Complexes
Ventricular Premature Complexes
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