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GE Vivid S60

GE Vivid S60
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Device labels
Vivid S70 / S60User Manual 2-27
BC092760-1EN 01
For USA only:
Caution: Federal law restricts this device
to sale by or on the order of a physician.
Rear of
system
N/A- by GE
Healthcare
TUV SÜD
Classification Label
Rear of
system
N/A- by
certification
body
Mark name: "Eurasian Conformity" mark;
the single conformity mark for circulation
of products on the markets of member-
states of Customs Union.
Mark meaning: This product passed all
conformity assessment (approval)
procedures that correspond to the
requirements of applicable technical
reguations of the Customs Union.
Rear of
system
N/A- by
certification
body
GOST-R Mark: per Law of the Russian
Federation No. 184-FZ.
Rear of
system
N/A- by
certification
body
Non-ionizing electromagnetic radiation. Rear of
system
IEC 60417-5140
Alternating current Various IEC 60417-5032
Protective earth (ground) Internal IEC 60417-5019
Equipotentiality: Indicates terminal to be
used for connecting equipotential
conductors when interconnecting
(grounding) with other equipment as
described in IEC60601-1.
Rear of
system
IEC 60417-5021
Follow instructions for use. Read and
understand all instructions in the User's
Manual before attempting to use the
ultrasound system.
Rear of
system
ISO 7010-M002
Symbol indicating that the Instructions for
Use are supplied in electronic form.
Rear of
system
ISO 7000-1641
CAUTION - Dangerous voltage: Used to
indicate electric shock hazards.
Rear of
system
ISO 7010-W012
Label Purpose Location
Standard

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