Some versions are equipped with a continually adjustable flow outlet for measuring and
adjusting the volume flow of the gas. The gas flows upwards against the weight of the
float. The float adjusts to a certain height, depending on the volume flow. The volume
flow is adjusted by a needle valve downstream of the flow gauge.
Some versions of the pressure regulator are equipped with an alarm feature on
the input connection. An alarm sounds if the inlet pressure drops below a specific
value (see marking on the alarm feature). Medical gas flows into the area
surrounding the pressure regulator during this process. Observe the safety
information for working with medical gases.
3
ABOUT THE INSTRUCTIONS FOR USE
3.1
Scope
These instructions for use are valid for the TESCOM EUROPE WegaMed with the part
number indicated on the last page of these instructions for use.
Certain versions may be subject to further instructions for use, in addition to these.
3.2
Target audience
•
These instructions for use are intended for anyone responsible for the installation,
operation or monitoring of the above valves and fittings.
•
Maintenance may only be performed by TESCOM EUROPE or companies authorised
by TESCOM EUROPE.
•
The operator has a duty to ensure that only personnel who are familiar
with the general practice and safety measures associated with working
with gases and gas valves and fittings, as well as with the fundamental
regulations with regard to occupational safety and accident prevention,
are permitted to work on the device. These personnel must also have
been taught how to handle this pressure regulator, and have read and
understood the instructions for use.
•
The design of the appliance, the accompanying documentation and the
marking are based on the assumption that the appliance will only be
installed, operated and monitored by trained and qualified personnel
and that the user is familiar with certain general characteristics of the
appliance. As such, the instructions, warnings and safety information
focus mainly on features that are particular to the TESCOM EUROPE
pressure regulator.
•
The accompanying documentation does not address various general
hazards and risks that should be obvious to qualified medical personnel.
These include the improper use of the equipment and the possible side
effects on patients in an unusual state of health.
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