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Air Pro
3000
Mod. P0712EM F3000 Plus Version
Aerosol therapy apparatus
We are pleased you have purchased our product and we thank you for your trust in us.
Read these instructions carefully and retain them for future reference.
Only use the apparatus as described in this manual.
INTENDED USE
Air Pro 3000 Plus Version
is a professional medical device whose intended use is the administration of medication
prescribed or recommended by your doctor for the treatment of breathing ailments. It can be used in health care
structures like hospitals, in home care and for hire. The product should be used by legally authorized medical personnel
(doctors, nurses and therapists), by the home therapist, or by the patients themselves under the guidance of qualified
medical personnel. It is highly recommended that the health professional and/or the patient read and understand the
use and maintenance information of this manual.
Carefully follow the user and maintenance instructions to ensure proper functioning and to extend the life of the device.
Air Pro 3000 Plus Version
is fitted with a knob to adjust the pressure (A3), and with pressure gauge (A6) to display the
set pressure value.
The device does not require lubrication, is manageable, simple to use, reliable, resistant and quiet.
Note: Use only original FLAEM accessories.
• Do not expose the device to particularly extreme temperatures.
• Do not place the device near sources of heat, in direct sunlight or in excessively hot rooms.
• Do not obstruct or put objects into the filter or its related housing in the device.
• Never obstruct the air vents located on both sides of the device.
• Always use it on a rigid surface that is clear of obstacles.
• Make sure there is no material obstructing the air vents before each use.
• Do not put any objects in the air vents.
• Repairs, including the replacement of the supply cord, are to be carried out by FLAEM authorised personnel only, by
complying with the information provided by the manufacturer.
• The average operating life of the compressor is 2000 hours approximately.
• WARNING: Do not modify this device without authorisation from the manufacturer.
• The Manufacturer, the Vendor and the Importer shall be held responsible for safety, reliability and performance only
if: a) the device is used in compliance with the instructions for use b) the wiring where the device is being used is in
compliance with safety regulations and current laws.
• Interactions: the materials used in contact with medication have been tested with a vast range of medications. However,
in view of the variety and continuous evolution of pharmaceuticals, interactions cannot be ruled out. We recommend
using the medication as soon as possible once it has been opened and preventing prolonged exposure in the nebuliser
cup.
• The manufacturer must be contacted about any problems and/or unexpected events concerning operation and for any
clarifications on use, maintenance/cleaning.
• Interactions: The materials used in the medical device are biocompatible in accordance with the provisions of Directive
93/42 EC and subsequent amendments. However, the possibility of occurrence of allergic reactions cannot be entirely
excluded.
• The amount of time required between preservation conditions and use is approximately 2 hours.
STANDARD EQUIPMENT INCLUDES:
A
Aerosol Device (main unit)
A1- Switch
A2- Air outlet port
A3- Pressure adjustment knob
A4- Nebulizer port
A5- Carrying handle
A6- Pressure gauge
A7- Power supply cord socket
A8- Power cord
C
Accessories
C1-
RF7 Dual Speed Plus Nebulizer
C1.1-
Lower part
C1.2- Nozzle
C1.3-
Upper part
C1.4-
Speed selector with valve system
C2 -
Mouthpiece with valve
C2.1-
Expiratory valve
C3-
Non-invasive adult nasal prong
C4-
Child mask
C5-
Adult mask
C6-
Nebulization manual control
B
Connection tube (main unit / nebuliser)
INSTRUCTIONS FOR USE
Before each use, clean hands thoroughly and clean the device as described in the section on “CLEANING,
SANITISATION, DISINFECTION, STERILISATION”. During use, it is advisable to protect yourself from any dripping.
It is recommended that each person use their own nebulizer cup and accessories to prevent risk of infection due
to contamination.
This device is suitable for the administration of medical substances and not, for which the administration via aer-
osol is foreseen; these substances are to be in any case prescribed by the Doctor. In case of too thick substances,
the dilution with a suitable physiological solution could be needed, according to the medical prescription.
1. Insert power supply cord (A8) into socket (A7) and then connect it to a mains outlet adequate to the device voltage. The
position of the socket must be such that the device can be easily unplugged from the mains network
2.
Pour the medication prescribed by the doctor into the bottom part (C1.1)
3. Close the nebuliser by turning the top (C1.3) clockwise.
click
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Summary of Contents for AirPro 3000 Plus
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