3-1
3
Installation and Setting
3.1 Installation
WARNING
Equipment assembly and refit (including correct protective grounding
connection) during life period must be carried out by maintenance
technicians whom are trained and licensed by the manufacturer, and
evaluated according to the specified IEC60601-1. Please contact the
company if you have any queries.
The software copyright for this equipment belongs to the manufacturer.
Unless explicitly authorized, any alteration, reproduction or sale by any
means or in any form by any organization or individual is prohibited.
All the analog equipment and digital facilities should be certified
according to the specified IEC standard (such as:IEC60950 Information
Technology Equipment Safety and IEC60601-1 Medical Electrical
Equipment Safety). Moreover, all equipment should be connected based
on the requirements of the valid version of the IEC60601-1 system.The
qualified individual responsible for connecting auxiliary equipment to
the input and output signal ports is also accountable for making the
system in accordance with the IEC60601-1 standard. Please contact the
company if you have any queries.
When this equipment combining with other electrical equipments forms
a combination with a special function, and the user cannot determine
whether there is an impending danger from each equipment
specification (such as a danger of electric shock due to aggregation of
current leakage), please contact the company or a specialist in the field
at the hospital, to guarantee that all equipment in the combination are
safe enough and will not be damaged.
Please make sure this equipment is securely fixed and positioned.
Positioning changes and severe shock can lead to minor changes in the
delivery accuracy.
NOTE
This equipment is in accordance with the EN 1789:2007+A2:2014
standard.
Содержание BeneFusion SP3 Vet
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