Penlon ESO 2, Руководство пользователя, Страница: 11 / 72

ESO 2 ICU Ventilator 5 User Manual
Restricted device
Only for use in COVID-19 pandemic
Only to be used for emergency ventilation
All adverse incidents must be reported to MHRA on
0800 731 6789.
The device is intended to provide controlled concentrations
and flows of gases to the patient.
The ventilator assembly is a pneumatically driven, software
controlled, multi-mode ventilator, designed for mechanical
ventilation of adult and paediatric patients
Environment
The device is suitable for use by a professional operator in
a professional healthcare facility and must be continuously
attended when in use.
Do not use the device near HF surgical equipment, or outside
the RF shielded room of a medical system for magnetic
resonance imaging where the intensity of EM disturbances is
high.
Indications for use of the device
The device is intended to provide continuous mechanical
ventilatory support. The device is a restricted medical device
intended for use by qualified trained personnel under the
direction of a physician. Specifically the ventilator is applicable
for adult and paediatric patients.
The device is intended for use by healthcare providers, i.e.
Physicians and Nurses, in intensive care applications.
Oxygen Monitor
The Oxygen Monitor is intended to continuously measure and
display the concentration of oxygen in breathing gas mixtures,
and is intended for adult and paediatric patients. The oxygen
monitor is an integral part of the ventilator.
The oxygen monitor is intended for use by health care
providers, i.e. Physicians and Nurses, for use with patients in
intensive care applications.
2. Purpose