Here are just some of the modules you can add to your SLE6000



The SLE6000 sees the introduction of a new Lunar™ interface, which incorporates a low-glare screen (in keeping with the increased emphasis on developmental care) whilst setting a new benchmark in usability.

  • The etCO2 waveform and digital value are shown in yellow and allow the user to compare CO2 trends with any ventilator parameter.

  • When the SpO2 module is added to the SLE6000, the screen can show an additional plethysmogram waveform. All data is trended for up to 14 days.

  • A single on/off button activates OxyGenie and allows for safe control of the FiO2 level, ensuring the patient remains within a particular range for the maximum possible time.

  • Switching to HFOV is a button-push away and doesn't require any changes to the patient circuit. Parameter controls have changed to reflect the new mode. The ‘Additional Parameters’ button can display secondary controls for this mode. Selecting any parameter activates the + and - keys to adjust the parameter value.

Key features & specifications

  • Ventilate patients up to 30 kg
  • Unique Lunar™ interface

  • Sharp 12.1’’ colour LED touch-screen
  • V/P, F/P, F/V loops available
  • Compact, single-box design
  • 3+ hour battery life (in all modes)
  • 14 day data trending – 20 parameters
  • Screen capture

  • Proximal flow sensor

  • Flow and pressure breath detection
  • Connectors: RS232, VGA, USB, Ethernet

SLE is an exclusive partner of GE Healthcare in India

Resources

The official name of the product is SLE 6000 H, 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.
WIPRO GE HEALTHCARE PVT LTD
No. 4, Kadugodi Industrial Area,
Bangalore 560067,
Karnataka, India
CIN: U33111KA1990PTC01606