Important Information; Conformity With The Requirements Of European Union Directives; Intended Use; Contraindications And Side-Effects - EKOM DK50 4VR/50/M Benutzerhandbuch

IMPORTANT INFORMATION

1. 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.

2. 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.

3. CONTRAINDICATIONS AND SIDE-EFFECTS

There are no contraindications or side-effects known.

4. SYMBOLS

The following symbols and marks are used in the User manual, on the device and its packaging:
General warning
Warning - risk of electric shock
Warning - compressor is controlled automatically
Warning - hot surface
General caution
Read the operating instructions
Refer to instruction manual
CE – marking
Medical device
Protecting earthing
Fuse
NP-DK50 4VR 50, DK50 2x4VR 110-AD-1_03-2022 6
IMPORTANT INFORMATION
03/2022