MIL'S PRO2XY, Инструкции по запуску и обслуживанию, Страница: 35 / 48

PRO
2
XY OXYGEN CONCENTRATOR
519211-22 33
EN
OXYGEN RECEIVERS
Service conditions : The service conditions are specified on the receiver identification plate.
The operating pressure should never exceed the service pressure.
Minimum and maximum temperatures must be respected.
Purpose of use : These are single pressure devices designed to contain oxygen 93% ± 2%.
Installation and maintenance:
The receiver must be installed in neutral, normal and current atmosphere and in places which are not likely to involve a rise in
temperature of the device exceeding the temperature of service; it must be connected to ground. Access for check must be easy.
Incidents are always possible (exhaust of valve, leakage on drain or valve, etc...) so it is better to avoid the installation of a device in
an attended site, or near fragile devices.
Fixing and fastening of receivers must be made while taking care to avoid all forced and tensions and to damp out all vibrations, even
non-visible.
The base of the receiver will have to support the weight of the receiver, including in situation of tests.
The equipment must not be modified without the manufacturer's prior approval.
Periodic inspection:
By application of decision BSEI 09-219 of December 15th, 2009, the owner is exempted to proceed to the periodic visits (40 months)
on the oxygen tanks of the concentrator PRO2XY.This measure is applicable in France. For the other countries, it is recommended to
contact the competent authorities about the applicable regulations.
PROCOM 2
►
See the technical manual of the PROCOM 2 attached to this manual.
TRAINING
In order to ensure perfect aptitude in the use of the oxygen concentrator for medical use, the MIL'S SAS Company offers its own
training for the use of this equipment. It is intended for users and technical personnel working on or near the oxygen concentrator
for medical use.
CLEANING
Do not use corrosive product
If the unit's system requires cleaning, use a soap solution and a clean cloth.
Then wipe well with a dry cloth.
For disinfection, use swabs soaked in a disinfectant solution.
Frequency: as required.
END OF LIFE OF THE MEDICAL DEVICE
In order to limit negative impacts on the environment and to save natural resources, all waste must be treated according to its
nature (recycling, recovery, incineration, landfill or other treatment for hazardous waste). In order to channel each waste to the
appropriate treatment route, it is essential that it is collected and sorted correctly.
The device must be dismantled, and the components must be handled according to the following requirements:
►
Metal and plastic waste
Metal and plastic waste must be recycled according to the collection channels in place.
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Oils
The oil, if contained in the device, must be collected with a suitable container and not spilled on the ground.
It must be recycled according to the collection channels in place.
►
Waste from health care activities with an infectious risk
The filtration components of the vacuum pumps including in vacuum plants and anaesthesia gas scavenging systems are components
that have an infectious risk (toxins, viruses, bacteria); they must be handled with safety equipment (masks, gloves) and packaged in
a container suitable for waste from health care activities with an infectious risk.
They must be recycled and collected according to the channels in place.