Operating, Transport And Storage Conditions; Information And Explanation Of Symbols - Sonova Unitron Stride B-PR User Manual

9. Operating, transport and storage
conditions
The product is designed such that it functions
without problems or restrictions if used as
intended, unless otherwise noted in these user
guides.
Please ensure to use, charge, transport and
store the hearing aids according to the following
conditions:
Use
Temperature
Maximum
+5° to +40°C
range
(41° to 104°F)
Recommended
+5° to +40°C
range
(41° to 104°F)
Humidity
Maximum 0% to 85% (non
range condensing)
0% to 60% (non
Recommended
condensing)
range
Atmospheric 500 hPa to 1060
pressure hPa
66
Charging Transport Storage
+5° to +40°C -20° to +60°C -20° to +60°C
(41° to 104°F) (-4° to 140°F (-4° to 140°F)
+7° to +32°C 0° to +20°C 0° to +20°C
(45° to 90°F) (32° to 68°F) (32° to 68°F)
0% to 85% (non 0% to 70% 0% to 70%
condensing)
0% to 60% (non 0% to 60% 0% to 60%
condensing)
500 hPa to 1060 500 hPa to 1060 500 hPa to
hPa hPa 1060 hPa
10. Information and explanation of
symbols
With the CE symbol, Sonova AG confirms that
this product – including accessories – meets the
xxxx
requirements of the Medical Devices Regulation MDR
2017/745 as well as the Radio Equipment Directive
2014/53/EU.
The numbers after the CE symbol correspond to the code
of certified institutions that were consulted under the
above-mentioned directives.
This symbol indicates that the products described in
these user instructions adhere to the requirements for
an applied part of Type B of EN 60601-1. The surface of
the hearing aid is specified as applied part of Type B.
Indicates the medical device manufacturer, as defined
in the Medical Device Regulation (EU) 2017/745.
Indicates the Authorized representative in the
European Community. The EC REP is also the importer
to the European Union.
This symbol indicates that it is important for the user to
read and take into account the relevant information in
these user guides.
Indicates that the device is a medical device.
Indicates the manufacturer's catalogue number so that
the medical device can be identified