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Tele-ICU 2.0 equips central and bedside medical teams with a near real-time remote patient monitoring and early intervention solution.The platform enables remote access and collaboration with highly experienced critical care physicians and nurses in order to provide the best possible care for the ICU patients. It also improves efficiency, collaboration, patient care, and cost of care while elevating overall satisfaction for patients and clinical teams.

Tele-ICU 2.0 solution

Tele-ICU 2.0 solution

RADIOLOGY VIEWER

Automatically retrieves episodic image diagnostics for a selected patient.

CARDIOLOGY VIEWER

Automatically retrieves episodic ECG diagnostics for a selected patient.

Patient Vitals

Automatically displays near real time waveforms data from a connected device in patient's room.

CENTRICITY HIGH ACUITY

Displays individual patient's chart with full capability to enter or change treatment Plan

PATIENT CARE MANAGEMENT

Displays a holistic view of a selected unit by hospital location & helps prioritize most critical patients.

LIVE AUDIO/ VIDEO

Enables an on-demand audio & video connectivity to a patient's room.

1. Kaushal A, Gupta S, Dewan S, et al. Changing paradigm of health care delivery system in developing world: India’s first e-ICU Critinext 26th Annual Congress of the European Society of Intensive Care Medicine, 2013. Abstract.
 

 2. Gupta S, Bag P, Dewan S, et al. Extending Tele-ICU/E-ICU to rationalize antibiotic usage in coronary care unit in Indian scenario. 26th Annual Congress of the European Society of Intensive Care Medicine, 2013. Abstract. 

Disclaimer

The official name of the product is Tele ICU 2.0, 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.

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JB01112IN December 2022