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EKOM DO 2.1 - Important Information; Conformity with the Requirements of European Union Directives; Intended Use; Contraindications and Side-Effects

EKOM DO 2.1
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DO 2.1
DO 2.1-10
NP-DO2.1_10_08-2018 - 2 - 08/2018
IMPORTANT INFORMATION
1. CONFORMITY WITH THE REQUIREMENTS OF EUROPEAN UNION DIRECTIVES
This product conforms to the requirements of the Medical Device Directive (93/42/EEC), and is
safe for the intended use if all safety instructions are followed.
2. INTENDED USE
Dental suction unit DO 2.1 - is the source of vacuum to provide suction in the dental surgery aspirates
waste from the patients mouth - via a tip connected to the cannule of the suction hose, through the
pneumatic control module and down to the separator, where the water and foreign matter is left behind,
leaving only air to be drawn (sucked) to the suction unit and exhausted away from the surgery’s
environment.
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. WARNINGS AND SYMBOLS
The following symbols are used in the user manual, device and its packaging to denote important
details and information:
General warnings
Danger, electric shock hazard
Read the user manual!
CE-marking
Caution! Hot surface
Ground connection
Terminal for ground connection
Alternating current
Handling mark on package FRAGILE
Handling mark on package THIS SIDE UP
Handling mark on package KEEP DRY

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