Bayer HealthCare MEDRAD Stellant Operation And Installation Manual page 9

Keep Dry (ISO 15223-1, 5.3.4).
Medical - General Medical Equipment As
To Electrical Shock, Fire, and Mechanical
Hazards Only In accordance with ANSI/
AAMI ES60601-1 (2005) + AMD 1 (2012)
CAN/CSA-C22.2 No. 60601-1 (2014)
Indicates that this device conforms to the
requirements of the European Medical
Device Directive 93/42/EEC.
Attention: Refer to warnings and cautions
on Instructions for Use packaged in each
carton. (ISO 15223-1, 5.4.4)
Warning: Indicates hazardous voltages.
(ISO 7010, W012)
Indicates alternating current. (IEC 60417,
5032)
Indicates scanner connection.
Identifies a terminal suitable for direct
current. (IEC TR 60878, 5031)
Indicates injector connection.
Identifies the Equipotential connection.
(IEC TR 60878, 5021)
Indicates separate collection for Electrical
and Electronic Equipment per Directive
2002/96/EC. Refer to the following website
for additional information:
www.weee.bayer.com
Indicates the ISI module is Class 1 medical
equipment as defined by IEC 60601-1
CLASS 1
standards.
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