Exergy Solutions Bertie, Быстрый старт

Страница: 12 / 52

Alberta E-Vent User Manual Version 1.3 June 3, 2020 5
▪
Electronics are housed in an all metal enclosure
to suppress Electrical Magnetic Interference
(EMI)
from surrounding devices and
environment.
▪
A membrane covers the user interface and
control box to facilitate Alberta E-Vent surface
cleaning, sterilization and prevent debris and
other materials from penetrating into the
enclosure
▪
A Splashguard for the Resuscitator Mechanism to
reduce the risk of contamination.
2.3. Disclosures / Deficiencies
▪
This is an emergency device. If the device
malfunctions and no immediate fix is available,
shut the machine off and immediately follow
standard patient care procedures and switch to
manual ventilation.
▪
Shelf life or durability testing has not been
conducted on the Alberta E-Vent.
▪
Oxygen, Heliox, and air supply are not supplied.
The Alberta E-Vent BVM draws air from the
surrounding environment and can be connected
to an externally titrated, blended and supplied
oxygen source. There is
no FiO2 indication or
alarm.
▪
Patient pathology determines who can use this
device and length of treatment time to avoid
post-use complications. The clinician must be
aware of all the Alberta E-
vent’s limitations
before authorizing its use. For example, the tidal
volume operational range is narrower than full-
featured ventilators and accommodates a
narrower range of patients.
▪
The Alberta E-Vent and its components are
provided in a clean condition and should be
disinfected before use by the professional
healthcare facilities using their own disinfection
methods and procedures.
-
BVMs and Ventilation Circuit hoses and
valves are supplied by the healthcare
facility.