Technical Specifications - NOVAFON power User Manual

6. TECHNICAL SPECIFICATIONS

6.1. SYMBOLS USED
Alternating current
Device of protection class II according to DIN EN 61140
Hz Hertz
KB Short-time duty
mA Milliampere
V Volt
Disposal according to the EU Directive on Waste Electrical and Elec-
tronic Equipment (WEEE)
Displays the manufacturer of the medical device according to the
EU Directives 90/385/EEC, 93/42/EEC and 98/79/EC. Displays the
manufacturing date of the medical device.
Displays the serial number of the manufacturer so that a specific
SN
medical device is identified
Type BF: A type BF (Body Floating, conductive contact with the body)
applied part/device is connected to the patient's body to transmit
electrical energy or an electrophysiological signal to or from the
body
30° C
Temperature limit: refers to the temperature limits to which the med-
5° C
ical device can be safely exposed.
93 %
%
Humidity limitation
15 %
1060 hPa
Atmospheric pressure limitation
700 hPa
Refer to instruction manual/booklet
General warning sign
6.2. TECHNICAL SPECIFICATIONS
• Operating conditions: 5 °C to 30 °C; 15% to 93% relative humidity, not
condensing; 700 hPa to 1060 hPa atmospheric pressure
• Storage/transport: -25 °C to 70 °C; up to 93% relative humidity, not
condensing; 700 hPa to 1060 hPa atmospheric pressure
• Nominal voltage: Primary 230V~, 50 Hz, 65mA; Secondary 17V~, 100Hz,
450mA
• Nominal frequency: 50 Hz
• Operating mode: KB 20/15 min
• Nominal consumption: 9.5W
• Product category: Medical device class IIa according to the Medical
Devices Directive (93/42/EEC)
• Manufacturer: NOVAFON GmbH, Daimlerstraße 13, 71384 Weinstadt
• Operating noise: maximum 70 dBA
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