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TROUBLE-SHOOTING
Switch off the device before any procedure and unplug the power cable from the socket.
PROBLEM
CAUSE
SOLUTION
The device does not work
The power cable has not been cor-
rectly inserted into the socket of the
device or the power socket
Correctly insert the power cable in sockets.
The device does not
nebulise or nebulises in-
sufficiently.
The medication has not been insert-
ed in the nebuliser.
Pour the right amount of medication in the nebu-
liser.
The nebuliser has not been properly
fitted.
Disassemble the nebuliser and reassemble it cor-
rectly as shown in the connection diagram on the
cover.
The nebuliser nozzle is clogged.
Disassemble the nebuliser, remove the nozzle
and perform cleaning operations Failure to re-
move medication deposits from the nebuliser af-
fects its efficiency and operation
Strictly comply with the instructions contained
in the CLEANING, SANITISATION AND DISINFEC-
TION chapter
The air pipe is not correctly connect-
ed to the device
Ensure the device’s accessories are properly con-
nected to the air intake (see connection diagram
on the cover).
The air pipe is bent, damaged or
twisted
Unwind the pipe and ensure it is not crushed or
punctured. If necessary replace it.
The air filter is dirty
Replace the filter
The apparatus is noisier
than usual
The pressure regulator is not correctly
inserted in its housing
Fully and properly insert the pressure regulator in
its housing
If after verifying the above mentioned conditions the device should not operate properly, contact your trusted retailer or the nearest
authorised FLAEM service centre.
SYMBOLS
Certification TÜV
CE Medical Marking ref. Dir. 93/42 EEC and subsequent
amendments
Serial number of device
Class II device
Manufacturer
Important: check the operating instructions
Type BF applied part
“OFF” for part of equipment
Alternating current
“ON” for part of equipment
Hazard: electrocution.
Consequence: Death.
Do not use device while taking a bath or shower
Complies with: European standard EN 10993-1
“Biological Evaluation of Medical Devices” and
European Directive 93/42/EEC “Medical Devices”.
Phthalates free. In conformity with Reg. (EC) no.
1907/2006
IP21
Enclosure protection rating: IP21.
(Protected against solid bodies over 12 mm. Protected
against access with a finger.
Protected against vertically falling water drops.)
Minimum and maximum room temperature
Minimum and maximum air moisture
Minimum and maximum atmospheric pressure
Содержание AirPro 3000 Plus
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