11
Mains connection 230 V~; 50 Hz; 230 VA
UK: 240 V~; 50 Hz; 240 VA
Saudi Arabia: 220 V~; 60 Hz; 220 VA
Expected
service life
1000 h
Operating
conditions
Temperature: +10 °C to +40 °C
Relative humidity: 10% to 95%
Ambient pressure: 700 to 1060 hPa
Storage and
transportation
conditions
Temperature: 0 °C to +60 °C
Relative humidity: 10% to 95%
Ambient pressure: 500 to 1060 hPa
Aerosol properties 1) Flow: 5.3 l/min
2) Aerosol delivery: 0.326 ml
3) Aerosol delivery rate: 0.132 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
wearing parts
Designation
Material
REF
IH 26 Kids year pack (contains
mouthpiece, silicone children’s
mask, silicone baby mask,
atomiser, compressed air
hose, filter)
PP/PVC/
silicone
601.19
Standard IH 26 year pack
(contains mouthpiece, nose-
piece, adult mask, children's
mask, atomiser, compressed
air hose, filter)
PP/PVC
601.28
Nasal douche
PP
601.37
Baby mask
PVC
601.31
Removable “giraffe”
PP/ PVC
164.182
Note
If the device is not used according to the instruc-
tions specified, perfect functionality cannot be gu-
aranteed! We reserve the right to make technical
changes to improve and develop the product. This
device and its accessories comply with the Eu-
ropean standards EN60601-1 and EN60601-1-2
(CISPR 11, IEC61000-3-2, IEC61000-3-3,
IEC61000-4-2, IEC61000-4-3, IEC61000-4-4,
IEC61000-4-5, IEC61000-4-6, IEC61000-4-7,
IEC61000-4-8, IEC61000-4-11) as well as EN13544-1
and are subject to particular precautions with regard
to electromagnetic compatibility. This device meets
the requirements of European Directive 93/42/EEC for
medical devices, as well as those of the Medizinpro-
duktegesetz (German Medical Devices Act).
NOTES ON ELECTROMAGNETIC COMPATIBILITY
• The device is suitable for use in all environments li-
sted in these instructions for use, including domestic
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.
13. Warranty and service
Beurer GmbH, Söflinger Straße 218, 89077 Ulm, Ger-
many (hereinafter referred to as “Beurer”) provides a
warranty for this product, subject to the requirements
below and to the extent described as follows.
The warranty conditions below shall not affect
the seller’s statutory warranty obligations which
ensue from the sales agreement with the buyer.
The warranty shall apply without prejudice to any
mandatory statutory provisions on liability.
Beurer guarantees the perfect functionality and com-
pleteness of this product.
The worldwide warranty period is 5 years, commencing
from the purchase of the new, unused product from
the seller.
