11
• Never obstruct the air vents located on both sides of the device.
• Always use it on a rigid surface that is clear of obstacles.
• Before every utilisation ensure the ventilation slits are not obstructed by any material.
• Do not put any objects in the air vents.
• Repairs, including the replacement of the power cable, are to be carried out by FLAEM authorised personnel only, by
complying with the information provided by the manufacturer. Unauthorised repairs void the warranty and may be
hazardous for the user.
• The average expected duration for the compressor series are: F400: 400 hours, F700: 700 hours, F1000: 1000 hours,
F2000: 2000 hours.
• ATTENTION: Do not modify this device without authorisation from the manufacturer.
• The Manufacturer, the Dealer 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 medications have been tested with a vast range of medications. How-
ever, in view of the variety and continuous evolution of medications, interactions cannot be ruled out. We recom-
mend 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 or cleaning.
• Interactions: The materials used in the medical device are biocompatible in accordance with the provisions of Direc-
tive 93/42 EC and subsequent amendments. However, the possibility of occurrence of allergic reactions cannot be
entirely excluded.
• The amount of time required to switch from preservation to operating conditions is approximately 2 hours.
OPERATING INSTRUCTIONS
Before each use, wash your hands accurately and clean the device as described in the paragraph “CLEANING, SAN-
ITISATION AND DISINFECTION”. During application, it is advisable to suitably protect yourself from any dripping.
The nebuliser cup and accessories are for personal use only to avoid potential risks of transmitting infection. This
device is suitable for the administration of medical and non-medical substances, prepared for administration via
aerosol. These substances must be, in any case, prescribed by a Doctor. With substances that are too thick, dilu-
tion with a suitable physiological solution could be needed, according to the medical prescription.
1. Insert the power cable (A6) into the socket (A5) situated at the back of the device and then connect it to a mains outlet
adequate for the device voltage. The position of the socket must be such that the device can be easily unplugged from
the mains network.
2. Assemble the nozzle as indicated in the “Connection diagram” in point C1.2. Insert the complete nozzle in the bottom
part (C1.1). Insert the exhalation valve (C1.4) in the upper part (C1.3) as shown in the "Connection diagram" in point C1.
3. Pour the medication prescribed by the doctor into the lower part (C1.1). Close the nebuliser by turning the upper part
(C1.3) clockwise.
4. Connect the accessories as indicated in the “Connection diagram” on the cover.
5. Sit comfortably holding the nebuliser in your hand, place the mouthpiece onto your
mouth or alternatively use the nose piece or mask. Should you opt for the mask acces-
sory, place it on your face as shown in the picture (with or without using the elasticated
strap).
6. Switch the device on by pressing the switch (A1) and gently take a deep breath; we
recommend holding your breath for an instant to allow the inhaled drops of aerosol to
deposit. Then exhale slowly.
7. When administration is finished, switch off the device and unplug it.
ATTENTION:
After the administration session, if a noticeable deposit of moisture forms in- side the pipe (B), detach the
pipe from the nebuliser and dry it with the very ventilation from the compressor. This operation prevents mould
from developing inside the pipe.
ENGLISH
Summary of Contents for NOVAMA NELLA P0406EM F400
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