Mindray Zonare ZS3, Service Manual

Page: 13 / 295

ZS3 Service Manual Page 13 of 295
Notes When Returning or Transporting the
System, Probes, and Repair Parts
When returning or transporting the ultrasound system in the original packaging, ensure
that:

The ultrasound system should be adjusted to its lowest height and the monitor
should be folded in the down position.

The control panel should be placed in the center and locked.
Note:
When you return the system, ensure that the system is fully decontaminated, and
human fluids or blood are removed from the system, parts or probes. This is to protect
those who transports, receives or opens this package.
The US Department of Transportation (DOT) has ruled that “items that were saturated
and/or dripping with human blood that are now caked with dried blood; or which were
used or intended for use in patient care” are “regulated medical waste” for transportation
purpose and must be transported as a hazardous material.
Warning & Cautions
It is extremely important to read the following definitions of WARNING information, prior
to beginning any service on any sub-system within the system. As you see applicability
of each of these noted WARNINGs, during the course of the servicing process, be
prepared to avoid harm to persons and equipment by proper adherence.
It is not possible to anticipate every condition and situation in which ultrasound system
will be used. The following warnings and cautions represent typical situations that
require special attention. User knowledge and experience with a specific application and
environment must also be taken into consideration in order to help ensure the safety of
personnel and equipment.
Safety Standards
All Mindray instruments, cables, and diagnostic ultrasound imaging transducers have
been designed to meet the essential requirements contained in 93/42/EEC (Medical
Device Directive), and all appropriate requirements contained within IEC 60601 -1,
AAMI STD ES 60601-1, CSA STD C22.2 NO. 60601-1 (Medical electrical equipment -
Part 1: General requirements for basic safety and essential performance), IEC 60601-2-
37 (Medical electrical equipment - Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment), IEC 60601-1-2 (Medical
electrical equipment - Part 1-2: General requirements for basic safety and essential
performance Collateral Standard: Electromagnetic Compatibility), including limits for