User Manual

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© 2019 Endotronix® Inc. 100469-00 Rev. 2
Device should be attached to direct current source.
Device should be attached to alternating current source.
The myCordella™ Patient Reader operates using lithium-
ion batteries. Lithium-ion batteries should not be
crushed or burned.
Equipment meeting the safety requirements specified for
Class II equipment according to IEC 61140.
Type BF applied part complying with IEC 60601-1.
IPN
1
N
2
Manufacturer-determined degree of particle and water
ingress protection, where...
N1 = degree of protection from particulates (scale of 0-6);
and
N2 = degree of protection from water (scale of 0-8)
IP21
Protected against solid foreign objects of 12.5 mm and
greater, and against the effects of dripping water.
IP22
Protected against solid foreign objects of 12.5 mm and
greater, and against the effects of dripping water when
tilted at 15°.
Device has been demonstrated to pose no known hazards
in a specified MRI environment with specified conditions of
use.
General warning.
Possibility of system damage, malfunction, or the delay in
treatment.
On/Standby button.
IEC 60417-5140 - Equipment includes RF Transmitter.
Federal Communication Commission Number.