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›
Instrukcje obsługi
›
Instrukcje FLAEM
›
Instrukcja Inhalator nebulizator pneumatyczny FLAEM Respir Air 0.23 ml/min
Znaleziono w kategoriach:
Inhalatory
(12)
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Instrukcja obsługi Inhalator nebulizator pneumatyczny FLAEM Respir Air 0.23 ml/min
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Wyświetl w osobnym oknie
Assembly diagram - Schéma de montage -
V
erbindingsschema
Anschlussschema - Schemat połączeń dla nomenklatury - схеме соединения
ENGLISH
pg. 2
FRANÇAIS
Pag. 7
NEDERLANDS
Pag. 12
DEUTSCH
Pag. 17
POLSKI
PÁG. 22
РУС
СКИЙ
CTp
. 27
INSTRUCTIONS FOR USE MANUAL -
Aerosol therapy unit for frequent use
MODE D’EMPL
OI -
Appareil aérosol pour utilisation fréquente
GEBRUIKSA
ANWIJZING -
Aerosol voor regelmatig gebruik
GEBRAUCHSANWEISUNG -
Aerosol-Inhalationsgerät für den häufigen Gebrauch
INSTRUK
CJA OBSŁ
UGI -
Aerozol urządzenie do częstego stosowania terapii
-
Аппарат для аэрозольтерапии, для частого использования
PL
D
A
B
C
A1
A2
C2
C3
C4
C2.1
A5
C1
A4
C1.4
C1.3
C1.2
C1.1
C1
A3
A6
2
Respirair
Mod.: P0611EM F1000
Aerosol T
herapy Device
Congratulations on y
our purchase and thank you for your condenc
e in us.
Our goal is to fully satisfy our customers by oering them
cutting-edge products for the treatment of respiratory tract ailments.
Please read these instructions carefully and keep them handy for future r
eference. U
se
this device only as described in this manual.
This is a medical device f
or home use for the
nebulization and administration of medication pr
escribed or suggested by your doctor
.
Please visit
www.aem.it
to see our entire r
ange of Flaem products
THIS DEVICE COMES EQUIPPED
WITH:
A - Aerosol Devic
e (main unit)
A1 - Switch
A2 - Air outlet port
A3 - Air lter
A4 - Nebulizer port
A5 - Carrying handle
A6 - Pow
er cord
B -
Connection tube
(main unit / nebulizer)
C - Acc
essories
C1 - RF7 Dual Speed Plus Nebulizer
C1.1 - Bottom piece
C1.2 - Nozzle
C1.3 -
T
op piece
C1.4 - Speed selector with valve system
C2 - Mouthpiece with valve
C2.1 - Exhalation valve
C3 - Pediatric mask
C4 - Adult mask
D -
Con
venient, roomy carrying bag
IMPOrT
AnT
SAFEgUArDS
•
Beforeusing
theunit
for
therst
time,and
periodically
throughoutits
life,check
the
powersupply
cordf
oranydamage;ifyou
detectanydamage,donotplug
itin.
T
aketheapplianceimmediately
to
an authorised service centre or your dealer
.
•
The
av
erage
lifespan
of
accessories
is
1
year;
however
,
we
recommend
you
replace
the
nebulizer
every
6
months
in
intensive
use
(or
earlier,if
the
nebulizer
is
blocked)
to
always
ensure
maximum
therapeutic eect.
•
Childrenand
disabled
persons
should
alwaysuse
the
unit
understric
t
supervision
of
an
adult
who
has read this manual.
•
Severalpartsofthedevicearesmallenought
obeswallowedby
children;therefore
keepthedevice
out of reach of children.
•
Do
not
use
the
tubes
and
the
cords
of
the
device
for
pur
poses
other
than
those
specied
as
they
may cause strangulation hazard; utmost att
ention must be paid to children and persons with special
needs;usually
,suchpersonsarenotcapableofassessingthehazardcorrectly
.
•
Theunitshouldnotbeusedinthepresenceofanaestheticmix
tureinammablewithair
,oxygenor
nitrous oxide
.
•
Keepthecordawa
yfromheatedsurfaces.
•
Keep
the
power
supply
cord
away
from
animals
(for
example
rodents)
as
they
may
damage
the
insulation of the power supply cor
d.
•
Do
not
handle
the
unit
with
wet
hands.
Do
not
use
the
device
in
humid
environments
(e.g.
while
takingabath
orshower).
Donotimmerse
thedevice
inwater;
shouldthisacciden
tallyoccur
,unplug
the device immediately
. Do not remove or touch the device immersed in w
ater before pulling out
the plug.
T
ake the device immediately to an authorized service center or t
o your local dealer
.
•
Onlyusethedeviceindust-freeenvir
onments;otherwise,therapymaybecompromised.
•
The
casing
of
this
unit
is
not
protected
against
the
penetration
of
liquids.
Do
not
wash
the
device
underrunningwaterorsubmergeinwat
er.Keepa
wayfromsplashingwaterorotherliquids.
•
Donotexposethedevicetohightemperatures.
•
Donotputthedevicenearheatsources,directsunlight,orinhotenvir
onments.
•
Donotobstruc
torinsertanyobjectsinthelterorinitshousinginthedevice.
•
Donotobstruc
ttheairventsplacedonbothsidesoftheunit.
ENGLISH
3
OPErA
TIng InSTrUCTIOnS
Before each use, clean hands thor
oughly and clean the device as described in the section on
“
CLEAnIng, SAnITIZA
TIOn AnD DISInFECTIOn”
. 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 pre
vent risk of infection due to contamination.
1.
Plugthepowercord(A6)
intoapowersocket
correspondingtothevoltage
oftheunit.Thismust
be
positioned so that it is not dicult to make the disconnection from the mains.
2.
Openthenebulizerbyturningthetoppiece(
C1.3)anticlockwise.
3.
Pour
the
medicine
prescribed
by
your
physician
in
the
bottom
piece
(C1.1).
Close
the
nebulizer
by
turningthetoppiece(C1.3)clockwise.
4. Connect accessories as indicated in the
“Connection diagram
”
on the cover
.
5.
Sit
comfortably
holding
the
nebuliser
in
your
hand,
place
the
mouthpiece
ont
o
your
mouth
or
alternatively use the nose piece
or
mask.
Should
you
opt
for
the
mask
accessory,
plac
e
it
on
your face as shown in the picture (with or without using the
elasticatedstrap).
6.
Turn
on
the
device
using
the
switch
(A1)
and
then
breathe
in
and exhale deeply
.
7.
When
thetreatment
is
nished,shut
o
the
deviceand
unplug
the power cord
.
W
ARNING: If after the therapy session moisture accumulates in
thetube
(B),removethe
tube
fromthe
nebulizerand
dry
itusing
the device’
s compressor fan; this operation will
prevent mold from
forming inside the tube.
•
Duringuse,alwaysplacetheunitonarmsurfaceclearofobstacles.
•
Checkthatthereisnomaterialobstructingtheairventsbefor
eeachuse.
•
Donotplaceanyobjectsinsidetheairvents.
•
Repairs
must
be
per
formed
by
authorized
personnel
only.
Any
unauthorized
repairs
will
void
the
warranty and may pose a safety hazard for the user
.
W
ARNING:Donotmodifythisequipmentwithoutauthorizationofthemanufacturer
•
Theaverage
duration
providedfor
compressor
rangesis:
F400:
400
hours,
F700:
700
hours,
F1000:
1000hours,F2000:2000hours.
•
The
Manufac
turer
,
the
Retailer
and
the
I
mporter
are
responsible
for
the
safety
,
reliability
and
performanceof
thedevic
eonly
if
:
a)the
deviceis
usedin
accordance
with
the
operating
instructions
b)theelectricalsystemof
thepremiseswherethedevic
eisusedisincomplianc
ewithcurrentlaws
.
•
Interactions:The
materials
used
that
comeinto
contact
with
medications
havebeen
tested
with
a
wide
range
of
medications.
However
,
due
to
the
variety
and
continuous
evolution
of
medication,
the possibility of a chemical interaction cannot be excluded.
We r
ecommend that once the
medication has been opened you should use it as soon as possible and avoid pr
olonged contact of
the medication with the nebulizer
.
•
The
manufacturershould
be
contactedf
orreporting
problemsand/or
unexpec
ted
events
related
to
device operation.
HOW
TO USE
THE
“rF7 DU
AL SPEED PL
US”
nEBULIZEr
WITH
SPEED SELECTOr AnD
V
AL
VE SySTEM
Prof
essionaland
fast,this
device
issuitable
foradministering
alltypes
ofmedications
,
including
more
expensive
ones,
ev
en
in
patients
with
chronic
diseases.
The
geometry of the internal lines of the RF7 Dual Speed Plus nebulizer ensures the ideal
granulometry for active treatment all the way down t
o the lower respiratory tract.
T
o
speed
up
the
inhalation
therapy,
mov
e
the
speed
selector
button
(C1.4)
by
pressing on MAX with y
our nger
.
Foramoreeectiveinhalationtherapy
,presson
theoppositesideof
thewordMax
located
on
the
speed
selector
button
(C1.4);
this
allows
you
to
inhale
an
optimal
amount of the medication and reduces dispersion of the medication int
o the
surrounding environment t
o a minimum thanks to the valve system provided in the
nebulizer
,mouthpiece,andmask.
MAX
4
SOFTTOUCH MASk
SoftT
ouch
masks have an outer edge made of
soft
biocompatible material
that ensur
es excellent adherence t
o
theface,andis
alsoequippedwithan
innovativ
e Dispersion
Limiting Device
.
These distinctive elements that distinguish
it allow greater sedimen
tation of medication in the patient
and also
limit dispersion
.
During
the
inspiratory
phase,
the
tab
,
acting as a
Dispersion Limiting Device
,
bends inwards to
wards the mask
During
the
expiratory
phase,
the
tab
,
acting
as
a
Dispersion Limiting
Device
,
bends
outwards
from
the
mask.
Soft
biocompatible
material
Dispersion
Limiting Device
CLEAnIng, SAnITIZA
TIOn AnD DISInFECTIOn
T
urn o the unit before any cleaning and disconnect the power cor
d from the mains.
CLEAnIng
THE DEVICE AnD THE
TUBE’S OUTEr SUrF
ACE
Onlyuse
aclothdampened
withantibacterialdeter
gent(non-abrasive
andfree
ofsolvents
ofany
kind).
SAnITIZA
TIOn AnD DISInFEC
TIOn OF
THE AC
CESSOrIES
We r
ecommend a personal use of both the nebulizer and accessories to avoid an
y risk of infection or
contagion.
Openthe
nebulizerbyrotatingthe
upperpar
t(C1.3)counter-clockwise,detach
thenozzle
bypressing
as indicated by the 2 arrow
s in the
“
Assembly diagram”
section C1.
SAnITIZA
TIOn
Before
and
after
each
use,
sanitize
the
nebuliz
er
and
accessories
according
to
one
of
the
methods
descrive below
.
(Method A):
The accessories tha
t can be sanitized with the method A are (C1.1-C1.2-C1.3-C1.4-
C2-
C3-C4)
.
Sanitize
the
accessories
in
warm
(approximately
40°
C)
drinking
water
with
mild
dishwashing
liquid(nonabrasive)orinthedishwasherwithhotcycle
(Method B): T
he accessories that can be sanitized with the method B are (
C1.1-C1.2-C1.3-
C1.4-
C2-C3-C4)
.
Sanitizetheaccessoriesbyimmersionin
asolutionconsistingof
60%waterand40%
white
vinegar
.Finallyrinsethoroughlywithwarm(appr
oximately40°C)drinkingwater
.
Aftersanitizationshake
theaccessories
vigorouslyandplace
themona
papertowel,oralternatively,
drythemwithajetofhotair(e.g.usingahairdryer).
DISInFECTIOn
The accessories tha
t can be disinfected are (C1.1-C1.2-C1.3-C1.4-
C2-C3-C4)
The disinfection procedure described in this parag
raph is to be performed before using the accessories
and is eective only if all the prescriptions herein ar
e met and all the components involved are pr
eviously
sanitized.
Thedisinfectanttobeusedmustbeofelectrolyticoxidizingchlorinetype,(activeingredient:
sodiumhypochlorite),specicfordisinf
ectionandisavailableinallpharmacies.
Procedure:
-
Fillacontainer
,suitable
tocontainalltheindividualcomponentstobe
disinfected,withasolutionof
drinking
waterand
disinfectant,whilerespec
tingthe
proportions
indicatedonthe
packaging
ofthe
disinfectant itself
.
-
Completelyimmerse
each
individual
component
in
the
solution,
taking
care
to
avoid
the
formation
of air bubbles in contact with the components. Lea
ve the components immersed for the period of
timeindicated
onthepackagingofthe
disinfectant,andassociat
edwiththeconc
entrationchosento
prepare the solution.
-
Remove the components now disinf
ected and rinse thoroughly with lukewarm drinking water.
-
Afterdisinfectionshakethe
accessoriesvigorouslyandplacethem
onapaper
towel,oralternatively
,
drythemwithajetofhotair(e.g.usingahairdryer).
-
Dispose of the solution as recommended by the disinf
ectant manufac
turer
.
5
Description
Code
-
RF7 Dual Speed Plus Nebulizer Set composed of:
nebulizer
,mouthpiecewithvalveandnosepiece
AC
O464P
-
1
m
connection
tube
AC
O35
-
MaskSetcomposedof
:adultmask,pediatricmaskandelasticband
AC
O462P
-
SpareAirlterkitperunit(2pcs)
AC
O439P
A
VAILABLE SP
ArE P
ArTS
AIr FIL
TEr
The
devicehas
a
suc
tion
lter
(A3)that
should
be
replaced
when
it
is
dir
ty
or
changes color
. Do not wash or reuse the same lter
. Regular replacement of
the
lteris
requiredto
helpand
ensure
correctperformance
ofthe
compressor
.
Check the lter on a regular basis. C
ontact your local dealer or authorized
service center for spare lters
.
Use original FLAEM accessories only
.
Class II device
Important: check the operating
instructions
“OFF” for part of equipment
“ON” for part of equipment
Complies with: European standar
d
EN 10993-1 “Biological Evaluation of
Medical Devices” and European
Directive 93/42/EEC “Medical Devices”
Serial number of device
SyMBOLS
T
ype BF applied part
Alternating current
Hazard: electr
ocution.
Consequence: Death.
Do not use device while taking a
bath or shower
CE Medical Marking ref. Dir
. 93/42
EEC and subsequent amendments
TÜV Certification
ref. EN 60601-1 3° Ed.
EN60601-1-11
Enclosure pr
otection rating: IP21.
(Protected against solid bodies over 12 mm.
Protected against access with a finger; pro-
tected against vertically falling water drops.)
IP21
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