Stryker Crossfire - EMC Emissions Declarations; Emissions Compliance and Environment

EN-12
If the Crossre™ System is used adjacent to or stacked with
other equipment, observe and verify normal operation
of the Crossre™ System in the conguration 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 Crossre™ System.
When the Crossre™ 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.
e 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 dicult
to disconnect the AC power cord.
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
The Crossre™ System is intended for use in the electromagnetic environment specied below. The
customer or the user of Crossre™ System should ensure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment
- Guidance
RF emissions CISPR11 Group 1 The Crossre™ System must emit
electromagnetic energy in order to
perform its intended function. Nearby
electronic equipment may be affected.
RF emissions CISPR11 Class A Crossre™ System is suitable for
use in all establishments other than
domestic and those directly connected
to the public low-voltage power supply
network that supplies buildings used
for domestic purposes.
Harmonic emissions IEC
61000-3-2
Class A
Voltage Fluctuations/icker
emissions IEC 61000-3-3
Complies