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Before initial use the product should be kept in its original packaging. The
manufacturer recommends use of the original packaging (including internal
sealing bag and caps) if the product is withdrawn from operation (for transport,
storage).
Statutory laws, rules and regulations for medical gases, accident prevention and
environmental protection must be observed.
Operation conditions
-20/+60 °C
10/100 %
600/1200 mbar
• In case of storage at a temperature below -20 °C, do not operate the
!
flow selector until it has been allowed to increase its temperature to a
minimum of -20 °C.
4. Personnel instructions and training
According to Medical Devices Directive 93/42/EEC the product owner must
ensure that all personnel handling the product are provided with the operating
instructions and performance data and are fully trained to carry out that opera-
tion. Trainees need to be supervised by an experienced person.
5. Product description
Gas from the medical gas pipeline system is entering through the inlet connec-
tor (A) that is connected to the gas outlet. Flow is then adjusted to the reque-
sted value by turning handwheel (B). The adjusted flow is visible in the window
of the handwheel. Gas is delivered to the user through the flow outlet user
connection (C).
A. Inlet quick connector (QC)
The low pressure regulator is fitted to the medical gas pipeline system terminal
unit or to medical regulator by a gas specific male probe.
B. Handwheel
Requested gas flow can be adjusted by the handwheel (l/min). By the hand
wheel is possible to close the gas flow – adjusting value "0".
A
EN - Instruction for use - Debistar
Storage and transport conditions
-30/+60 °C
10/100 %
600/1200 mbar
B
C
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