EN-56
DRAFT
When the Crossre2 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. Any Type CF applied part should be used
together with other Type CF 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 dicult to disconnect the AC power cord.
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
The Crossre2 System is intended for use in the electromagnetic environment specied below. The
customer or the user of Crossre2 System should ensure that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment - Guidance
RF emissions CISPR11 Group 1 The Crossre2 System must emit
electromagnetic energy in order to
perform its intended function. Nearby
electronic equipment may be aected.
RF emissions CISPR11 Class A Crossre2 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
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