Technical Specifications - Beurer IH 40 Instructions For Use Manual

Problem/ Possible cause/remedy
question
There is inha- This is normal and is necessary for
lation solution technical reasons. Stop the inhalation
residue in the as soon as you can no longer detect
medication nebulisation or the device switches off
container. automatically due to a lack of inhalant.
What should 1. On babies, the mask should cover
be taken into the mouth and nose to ensure ef-
account when fective inhalation.
using the de- 2. On children, the mask should also
vice with ba- cover both the nose and mouth. It is
bies and chil- not a good idea to carry out nebuli-
dren? sation on someone who is sleeping,
as in this case not enough of the
medication will reach the lungs.
Note: Inhalation should only be car-
ried out under the supervision of an
adult and with their assistance and
the child should not be left alone.
Does inhala- This is necessary for technical rea-
tion using the sons. You breathe less medication
mask take per breath through the holes of the
longer? mask than via the mouthpiece. The
aerosol is mixed with ambient air via
the holes.
Should each Yes, this is absolutely essential.
person have
their own at-
omiser?

11. Technical specifications

Dimensions
(LxWxH) 201 x 147 x 141 mm
Weight 315 g incl. batteries
Filling volume Medication container max. 8 ml
Water tank max. 20 ml
Medication flow rate approx. 0.4 ml/min.
Ultrasonic transduc-
er frequency 1.7 MHz
Housing material ABS
Power supply 100 – 240 V ~, 50 – 60 Hz; 0.15 A
DC output: 13.5 V, 1 A
Operating condi- Temperature: +5 °C to +40 °C
tions Relative humidity: < 85% non-con-
densing
Storage and trans- Temperature: -20 °C to +70 °C
portation conditions Relative humidity: < 95% non-con-
densing
Subject to technical changes.
Wearing parts are excluded from the guarantee.
Replacement items
Name
Medication container
Year pack
(contains mouthpiece,
adult mask, children's
mask, connector for
masks, 12 medication
containers, hose, re-
placement filter)
100
50
0
1 10
The measurements were carried out with a sodium
chloride solution using a laser diffraction method.
The diagram may therefore not be applicable to sus-
pensions or highly viscous medications. You can ob-
tain more detailed information from the manufacturer
of your medication.
Note
If the device is not used according to the instructions
specified, perfect functionality cannot be guaran-
teed! 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 and
EN13544-1 and is subject to particular precautions
with regard to electromagnetic compatibility. Please
note that portable and mobile HF communication
systems may interfere with this unit. More details can
be requested from the stated Customer Services ad-
dress or found at the end of the instructions for use.
This device meets the requirements of European Di-
rective 93/42/EC for medical products, as well as
those of the Medizinproduktegesetz (German Medi-
cal Devices Act).
20
Material
PET
PP, PVC, EVA, PET
100
particle diameter (µm)
REF
163.373
601.07
1000