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6 TECHNICAL DATA
6.1 General
Electrical connection
Alternating current
100 – 240 V / 50 – 60 Hz / 0.5 – 1.1 A
Housing dimensions (W x H x D)
100 mm x 80 mm x 230 mm
Weight
606 g
Temperature of the medication solution used after
heating
max. 92 °C
Aerosol temperature at the mouthpiece
max. 43 °C
Minimum flow
3.0 l/min
Corresponding minimum operating pressure
0.5 bar / 50 kPa
Maximum flow
6.0 l/min
Corresponding maximum operating pressure
2.0 bar / 200 kPa
Minimum fill volume
5 ml
Maximum fill volume
15 ml
Operating gases
Air, oxygen
Aerosol data according to DIN EN 3544-1 is available on request from PARI GmbH or
on the Internet at www.pari.de/en/products (under "Technical data" on the respective
product page).
6.2 Classification according to DIN EN 60601-1
Type of electric shock protection
Protection class II
Degree of protection from electric shock of the part used (neb-
uliser)
Type BF
Degree of protection against water ingress in accordance with
EN 60529 (IP rating)
No protection
Degree of protection when used in the presence of flammable mix-
tures of anaesthetics with air, with oxygen, or with nitrous oxide
No protection
Operating mode
Continuous operation
6.3 Information about electromagnetic compatibility
Electrical medical equipment is subject to special precautionary measures with regard
to electromagnetic compatibility (EMC). Such equipment must only be installed and
operated in accordance with EMC instructions.
Portable and mobile high-frequency communication devices can disrupt electrical med-
ical equipment. Using accessories, converters and power cords other than those spec-
ified, with the exception of converters and power cords that the manufacturer of the
medical electrical device sells as spare parts for internal components, can result in
higher emission levels or lower the resistance to interference of the device.
