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EKOM DK50-10 - Important Information; Conformity with the Requirements of European Union Directives; Intended Use; Contraindications and Side-Effects

EKOM DK50-10
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DK50-10
NP-DK50-10-16_01-2022-MD - 6 - 01/2022
IMPORTANT INFORMATION
CONFORMITY WITH THE REQUIREMENTS OF EUROPEAN UNION DIRECTIVES
This product conforms to the requirements of the Regulation (EU) on medical devices (MDR
2017/745) and is safe for the intended use if all safety instructions are followed.
INTENDED USE
The compressor is used as a source of clean, oil-free compressed air to power active medical
devices where the parameters and properties of the compressed air are suitable for the specific
application.
Compressed air supplied by the compressor is unsuitable for use with artificial lung
ventilation devices without further filtration.
Any other use of the product beyond its intended use is considered an incorrect use. The
manufacturer is not liable for any damages or injuries resulting from the incorrect use.
CONTRAINDICATIONS AND SIDE-EFFECTS
There are no contraindications or side-effects known.
WARNINGS AND SYMBOLS
The following symbols are used in the user manual, device and its packaging to denote important
details and information:
General warnings
Warning
Danger, electric shock hazard
Read the user manual!
Refer to instruction manual
CE-marking
Medical device
Serial number
Compressor is controlled automatically and may start without warning
Caution! Hot surface

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