Technical Specifications - Beurer IH 55 Gebrauchsanweisung

Operation with mains part
The mains part must only be connected to the mains volt-
age that is specified on the type plate.
• Power supply: 100–240 V~; 50–60 Hz; 0.15 A
• Insert the mains part connector plug
(A) into the provided connector sock-
et (B) and fully insert the mains part
into a suitable socket.
Note
• Ensure that there is a mains socket close to the set-
up area.
• Arrange the mains cable so that no-one will trip over it.
• To disconnect the device from the mains after inhala-
tion, first switch the device off and then pull the mains
plug out of the socket.
• The batteries do not need to be removed during oper-
ation with the mains part.
• The mains part cannot be used for charging batteries.

10. Technical specifications

Dimensions
(LxWxH) 146 x 51 x 85 mm
Weight 228 g incl. batteries
Battery-operated 4 x 1.5 V type AA, Mignon (LR6)
Filling volume Max. 10 ml
Medication flow rate Approx. 0.25 ml/min.
Vibration frequency 100 kHz
Housing material ABS
Operating condi- Temperature: +10 °C to +40 °C
tions Relative humidity: < 93% non-con-
densing
Atmospheric pressure:
860 to 1060 hPa
Storage and trans- Temperature: -20 °C to +70 °C
portation conditions Relative humidity: < 93% non-con-
densing
Atmospheric pressure:
860 to 1060 hPa
Subject to technical changes. Wearing parts are excluded
from the guarantee.
B
A
The measurements were carried out with a sodium chloride
solution using a laser diffraction method.
The diagram may therefore not be applicable to suspen-
sions or highly viscous medications. You can obtain more
detailed information from the manufacturer of your med-
ication.
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 Europe-
an standards EN60601-1, EN60601-1-2 and EN13544-1
and are 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 address or found at the end of the in-
structions for use. This device meets the requirements of
European Directive 93/42/EEC for medical devices, as well
as those of the Medizinproduktegesetz (German Medical
Devices Act).
ELECTROMAGNETIC COMPATIBILITY
• The device complies with the currently valid require-
ments relating to electromagnetic compatibility and is
suitable for use in all buildings, including those desig-
nated for private residential purposes. The radio fre-
quency emissions of the device are extremely low and
are very unlikely to cause interference with other devic-
es in the vicinity.
21
Note