Guidance and Manufacturer’s Declaration 18-1
18
Guidance and Manufacturer’s
Declaration
The system complies with the EMC standard IEC60601-1-2: 2007.
WARNING:
The use of unapproved accessories may diminish system
performance.
NOTE:
1 Use of accessories, probes, and cables other than those specified may result in
increased emission or decreased immunity of system.
2 The system or its components should not be used adjacent to or stacked with other
equipment. If adjacent or stacked use is necessary, the system or its components
should be observed to verify normal operation in the configuration in which it will be
used.
3 The system needs special precautions regarding EMC and needs to be installed and
put into service according to the EMC information provided below.
4 Other devices may interfere with this system even though they meet the requirements
of
CISPR
.
5 Preventing conducted RF immunity. Due to technological limitations, the conducted RF
immunity level are limited to 1Vrms level, conducted RF interference above 1Vrms
may cause wrong diagnosis and measurements. We suggest that you position system
further from sources of conducted RF noise.
6 Operation of system, in the case that the patient physiological signal is lower than the
minimum amplitude or value specified in the product specifications, may cause
inaccurate results.
7 Portable and mobile RF communications equipment can affects system. See tables 1,
2, 3, and 4 below.
Summary of Contents for DC-T6
Page 1: ...DC T6 Diagnostic Ultrasound System Operator s Manual Basic Volume...
Page 2: ......
Page 10: ......
Page 16: ......
Page 28: ......
Page 37: ...System Overview 2 9 2 6 Introduction of Each Unit...
Page 178: ......
Page 182: ......
Page 236: ......
Page 240: ...13 4 Probes and Biopsy No Probe Model Type Illustration 19 CW2s Pencil probe...
Page 300: ......
Page 314: ......
Page 320: ......
Page 326: ......
Page 330: ...C 4 Barcode Reader...
Page 337: ...Barcode Reader C 11...
Page 342: ......
Page 347: ...P N 046 001523 01 V1 0...