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Advanced
Heavy duty highly automated device
Easy and intuitive operation
Portable device, does not require installation
A device for emergency ventilation and intensive care that allows you to control and monitor key ventilation parameters
Accuracy and safety
A device for emergency ventilation and intensive care that allows controlling and monitoring key ventilation parameters.
It has been designed to work continuously and intensively. It has different ventilation modes, providing it with great versatility to treat patients in different phases of invasive ventilation.
Control by SIEMENS PLC with a very simple and intuitive interface for maximum safety
Volume sensor and airway pressure on each side for added comfort
The device has sensors to control the values of air volume, pressure and flow provided to the patient, a security system with alerts and does not require installation.
Sensor calibration adjustment using an advanced mode.
Possibility of incorporating a FiO2 sensor
In addition, RESPIRA allows an external FiO2 sensor to be incorporated into the circuit for the measurement of% oxygen.
Different ventilation modes
Reading of tidal volume, pressure and flow provided to the patient remotely
Security control with alarm system
Graphs display in real time
Control of delivered tidal volume
The tidal volume administered to the patient is adjusted by controlling the stroke of the actuator that exerts compression on the resuscitating bag. The tidal volume range that can be provided to the patient goes from 180 mL to 880 mL.
I:E ratio
RESPIRA allows to perfectly assist human ventilation by adjusting expiration time to obtain the desired inspiration/expiration ratio. Expiration can be varied from 1 to 3 by 0.5.
Ventilatory frequency
The system controls the respiratory rate between 10 and 30 rpm (up to 45 rpm in assisted modes).
PEEP
The PEEP value set in screen electronically validates the value set in the mechanical PEEP valve.
Real-time parameter display
– Inspiratory tidal volume
– Inspiration and expiration pressure
(maximum, plateau and minimum)
– Respiratory rate
– Oxygen supply via FiO2 sensor with independent display (optional)
Visualization of graphs in real time
– Inspiratory flow
– Inspiration and expiration pressure
– Tidal volume
It has different modes of ventilation to treat patients in different phases of invasive ventilation
Volume Controlled
Ventilatory mode indicated for sedated patients. The device delivers airflow according to the parameters configured by the healthcare professional. This mode includes the option of insufflation self-adjustment to avoid out-of-range ventilatory parameters.
Volume Assisted
Weaning technique in which the established tidal volume is administered only when a patient’s inspiratory effort is detected. The patient is the one who marks the ventilatory frequency, but if the time interval between inspiratory efforts is greater than the preset apnea time, the device automatically switches to Volume Control. This mode includes an optional insufflation and I:E ratio self-adjustment avoid out-of-range parameters.
Volume Assist-Control
Ventilation mode intended for weaning. Airflow is delivered according to the parameters configured by the health professional. When the device detects a patient’s inspiratory effort during the expiratory phase of ventilation, a new ventilation cycle is initiated. With this technique, the device is adapted to a greater demand for inspirations than scheduled. This mode includes an optional insufflation and ventilatory frequency to avoid out-of-range parameters.
Self-adjustement
Additionally, RESPIRA has a smart mode that automatically adjusts the tidal volume and pressures to the previously set target values.
Trigger
RESPIRA allows you to adjust the trigger sensitivity (-1, -2, -3 cmH2O) with respect to PEEP.
Security system with alerts
The software incorporates an alert system that shows incidents or deviations in the breathing parameters on the device screen, as well as a loudspeaker that alerts you to such incidents.
See the list of alarms in the catalog attached below.
Download in pdf
Developed together with
With the collaboration and participation of
WARNING: Although we are working on the CE certification and conformity of the RESPIRA device, it does not satisfy the legal requirements of the EU yet. Therefore, the RESPIRA device is nowadays a product not destined for the European Union market and it is not intended to come onto EU market or to be placed in service in the EU until it meets the EU legal requirements.
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