GE Medical Systems LOGIQ ?200, Руководство по обслуживанию, Страница: 31 / 212

GE MEDICAL SYSTEMS
LOGIQ
α
200 SERVICE MANUAL
2138853
INTRODUCTION
1–15
REV 0
1–2–1 Warnings (Continued)
The following table describes the purpose and location of safety labels and other important information provided
on the equipment.
Label/Icon Purpose/Meaning Location
Identification and Rating Plate Manufacturer’s name and address
Date of manufacture
Model and serial numbers
Electrical ratings (Volts, Amps, phase, and
frequency)
Rear of console near power inlet
Type/Class Label Used to indicate the degree of safety or protec-
tion.
IP Code
(IPX1)
Indicates the degree of protection provided
by the enclosure per IEC 529. IPX1
indicates drip proof. Foot Switch
Equipment Type BF (man in the box symbol)
IEC 878-02-03 indicates B Type equipment
having a floating applied part. Probe connectors
Equipment Type CF (heart in the box
symbol) IEC 878-02-05 indicate equipment
having a floating applied part having a
degree of protection suitable for direct
cardiac contact. ECG connector and surgical probes
Device Listing/
Certification Labels Laboratory logo or labels denoting
conformance with industry safety standards
such as UL or IEC. Rear of console
“DANGER – Risk of explosion used
in...” The system is not designed for use with
flammable anesthetic gases. Rear of console
“CAUTION” The equilateral triangle is usually
used in combination with other symbols to
advise or warn the user. Various
“ATTENTION – Consult accompanying
documents” is intended to alert the user to
refer to the operator manual or other
instructions when complete information
cannot be provided on the label. Various