CardioDay 2.5 Holter ECG

Analytical Speed 

 

CardioDay harnesses the speed and standardization of automation while still enabling technicians to control the fine points of study analysis. Data is presented graphically with a visual clarity that enables quick, intuitive operation. 

 

CardioDay Holter ECG provides guidance through the analysis process, enabling fast-turnaround and consistent results. Data is presented visually in graphs and charts that highlight relevant trends, critical events, artifacts, and other key insights so users can move quickly and confidently through each study.

Clinical Confidence  

 

GE’s proprietary, clinically-proven algorithms have long been the clinicians’ choice for accuracy and consistency. CardioDay’s new functionality enhances analytical ease for critical sub-groups, including patients with atrial fibrillation (AFib), those at risk of sudden cardiac death, and patients with pacemakers.  

 

GE Healthcare has been setting the mark for clinical validity and excellence in ECG analysis since the 1980s. Today our suite of analysis programs are the preferred choice for clinicians and we continue to lead developments in computerized ECG analysis, setting even higher levels of clinical accuracy, validity, and performance—all available to you through CardioDay Holter ECG software.

Streamlined End-To-End Workflow 

 

CardioDay is the only Holter ECG system compatible with GE Holter recorders, bedside monitors, telemetry, and MUSE™ systems – delivering a streamlined end-to-end workflow solution that helps save time and reduce errors. 

 

An integrated cardiac care continuum is critical for efficient, high quality care delivery. CardioDay supports that ecosystem as the only Holter ECG system that optimizes your process – from orders to final report storage — by fully integrating with MUSE, GE Holter recorders, and GE bedside monitors and telemetry.

The official name of the product is Cardioday, authorized by Wipro GE HealthCare Pvt. Ltd., located at No 4, Kadugodi Industrial Area, Whitefield, Bangalore, Karnataka – 560067. The system is intended for use by trained healthcare professionals familiar with relevant clinical workflows and equipment operation. For safe and effective operation, users must verify system calibration, ensure correct supply and connectivity, and confirm settings appropriate to the patient’s clinical condition. Continuous monitoring of patient vitals and system performance is essential throughout use. This system must not be used in environments containing explosive gases or on patients with contraindications to its intended clinical use. Operators must follow all institutional protocols, manufacturer instructions, and established clinical guidelines. This material was created and reviewed on 22nd December 2025, and additional product and safety information is available upon request.