Replacement Parts And Wearing Parts - Medel AIR PLUS Manual De Instrucciones

Medication flow
rate Approx. 0.3 ml/min
Filling volume Min. 2 ml
Nasal douche Max. 10 ml
Sound pressure Approx. 52 dBA
(acc. to DIN EN 13544-1 section 26)
Power supply 230 V~; 50 Hz; 230 VA
UK: 240 V~; 50 Hz; 240 VA
Saudi Arabia: 220 V~; 60 Hz; 220 VA
Expected service
1000 h
life
Operating Temperature: +10°C to +40°C
conditions Relative humidity: 10% to 95%
Ambient pressure: 700 to 1060 hPa
Storage and Temperature: 0°C to +60°C
transportation Relative humidity: 10% to 95%
conditions Ambient pressure: 500 to 1060 hPa
Aerosol properties 1) Flow: 5.3 l/min
2) Aerosol delivery: 0.11 ml
3) Aerosol delivery rate: 0.07 ml/min
4) Particle size (MMAD): 3.07 µm
The serial number is located on the device or in the
battery compartment.
Subject to technical changes.
Particle size diagram
Measurements were performed using a sodium fluoride
solution with a "Next Generation Impactor" (NGI).
The diagram may therefore not be applicable to sus-
pensions or highly viscous medications. You can obtain
more detailed information from the manufacturer of
your medication.
12. Replacement parts and wea-
ring parts
Designation
Year pack AIR PLUS
Standard contains:
Mouthpiece
Nosepiece
Adult mask
Children's mask
Nebulizerer
Compressed air hose
Filter
Yearpack AIR PLUS Kids
contains:
Mouthpiece
Silicon children mask
Silicone baby mask
Angled fitting
Nebulizer
Compressed air hose
Filter
Note
If the device is not used according to the instructions
specified, perfect functionality cannot be guaranteed!
We reserve the right to make technical changes to
improve and develop the product. This device and
its accessories comply with the European standards
EN60601-1, EN60601-1-2 (CISPR 11, IEC61000-
3-2, IEC61000-3-3, IEC61000-4-2, IEC61000-4-
3, IEC61000-4-4, EC61000-4-5, IEC61000-4-6,
IEC61000-4-7, IEC61000-4-8, IEC61000-4-11) and
EN13544-1 and are subject to particular precautions
with regard to electromagnetic compatibility. This de-
vice meets the requirements of European Directive
93/42/EEC for medical products, as well as those of the
Medizinproduktegesetz (German Medical Devices Act).
NOTES ON ELECTROMAGNETIC COMPATIBILITY
• The device is suitable for use in all environments
listed in these instructions for use, including domes-
tic environments.
• The use of the device may be limited in the presence
of electromagnetic disturbances. This could result in
issues such as error messages or the failure of the
display/device.
• Avoid using this device directly next to other devices
or stacked on top of other devices, as this could lead
to faulty operation. If, however, it is necessary to use
the device in the manner stated, this device as well
as the other devices must be monitored to ensure
they are working properly.
• The use of accessories other than those specified
or provided by the manufacturer of this device can
34
Material REF
PP/Silicone
PP/Silicone
PVC/Aluminum 603.33
PVC/Aluminum
PP/Silicone
PVC
PU
PP/Silicone
Silicone/PP
Silicone/PP 603.34
PP
PP/Silicone
PVC
PU