Beurer IH 28 Pro Gebrauchsanweisung Seite 26

12. DISPOSAL
For environmental reasons, do not dispose of the
device in the household waste.
Please dispose of the device in accordance
with EC Directive – WEEE (Waste Electrical
and Electronic Equipment).
If you have any questions, please contact the local
authorities responsible for waste disposal.
13. TECHNICAL
SPECIFICATIONS
Model IH 28 Pro
Type IH 28
Dimensions
(W x H x D) 210 x 210 x 94 mm
Weight 1.65 kg
Operating
pressure Approx. 0.5 to 1.45 bar
Atomiser filling Max. 8 ml
volume Min. 2 ml
Medication
flow rate Approx. 0.35 ml/min
Sound
pressure Approx. 52 dBA
Mains 230 V~; 50 Hz; 230 VA
connection UK: 240 V~; 50 Hz; 240 VA
Operating Temperature: +10 °C to +40 °C
conditions Relative humidity: 15% to 93%
Ambient pressure:
700 to 1060 hPa
Storage and Temperature: -25 °C to +70 °C
transportation Relative humidity: 10% to 95%
conditions Ambient pressure:
700 hPa to 1060 hPa
Aerosol values 1) Aerosol delivery: 0.11 ml
accord- 2) Aerosol delivery rate:
ing to EN 0.07 ml/min
27427:2019 3) Fill volume dispensed in per-
based on adult cent per min. 3.5%
breathing 4) Residual volume: 1.68 ml
patterns with 5) Particle size (MMAD): 3.07 μm
sodium fluo- 6) GSD (geometrical standard
ride (NaF): deviation): 2.03
7) RF (respirable fraction < 5 μm):
75%
8) Large particle range (>5 μm):
25%
9) Medium particle range (2 to
5 μm): 47.8%
10) Small particle range (<2 μm):
27.2%
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 Impac-
tor" (NGI).
The diagram may therefore not be applicable to
suspensions or highly viscous medications. You
can obtain more detailed information from the
manufacturer of your medication.
14. WARRANTY/SERVICE
Further information on the warranty and warran-
ty conditions can be found in the warranty leaflet
supplied.
Notification of incidents
For users/patients in the European Union and
identical regulation systems (EU Medical Device
Regulation (MDR) 2017/745), the following applies:
If a major incident occurs during or through use of
the product, notify the manufacturer and/or their
representative of this as well as the respective na-
tional authority of the member state in which the
you are located.
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