Stryker Crossfire Bedienungsanleitung Seite 16

Guidance and Manufacturer's Declaration: Electromagnetic Emissions
The Crossfire™ System is intended for use in the electromagnetic environment specified below. The
customer or the user of Crossfire™ System should ensure that it is used in such an environment.
Emissions Test
RF emissions CISPR11
RF emissions CISPR11
Harmonic emissions IEC
61000-3-2
Voltage Fluctuations/flicker
emissions IEC 61000-3-3
EN-12
If the Crossfire™ System is used adjacent to or stacked with
other equipment, observe and verify normal operation
of the Crossfire™ System in the configuration in which
it will be used prior to using it in a surgical procedure
as interference may occur. Consult the tables below for
guidance in placing the Crossfire™ System.
When the Crossfire™ System is interconnected with other
medical electrical equipment, leakage currents may be
additive. To minimize total patient leakage current, any
Type BF applied part should be used together with other
Type BF applied parts. Ensure all systems are installed
according to the requirements of IEC 60601-1-1.
The separable AC power cord is provided as a means of
emergency shutdown and disconnection from the power
source. Do not position the console in a way that is difficult
to disconnect the AC power cord.
Compliance
Group 1
perform its intended function. Nearby
electronic equipment may be affected.
Class A
Class A
domestic and those directly connected
to the public low-voltage power supply
Complies
Electromagnetic Environment
- Guidance
The Crossfire™ System must emit
electromagnetic energy in order to
Crossfire™ System is suitable for
use in all establishments other than
network that supplies buildings used
for domestic purposes.