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Vers. 20210510ENG Page 11
2.8 Electromagnetic Compatibility Statement
❖ This equipment complies with GB/T18268.1–2010 (IEC61326–1:2005, IDT )
"Electromagnetic compatibility requirements for electrical equipment for measurement,
control and laboratory – Part 1: General requirements" and GB/T18268.26–2010
(IEC61326–2–6:2005, IDT ) Electromagnetic compatibility requirements for electrical
equipment for measurement, control and laboratory use Part 26: Particular
requirements for in vitro diagnostic (IVD) medical equipment.
❖ The following usage requirements should be strictly observed during use, otherwise
electromagnetic interference may be caused to other equipment or the electromagnetic
interference resistance of the equipment may be reduced or even the basic
performance may be lost.
❖ This equipment is designed and tested according to Class A equipment in GB4824. In
a domestic environment, this equipment may cause radio interference and precautions
may be required.
❖ Portable and mobile RF communications equipment may affect the description of
medical electrical equipment: Portable and mobile RF communications equipment may
affect the normal operation of this equipment, and portable and mobile RF
communications equipment should be guaranteed to meet certain spatial distances.
See Appendix A, “Recommended Isolation Distances Between Portable and Mobile RF
Communications Equipment and Equipment.”
❖ It is recommended to evaluate the electromagnetic environment before the equipment
is used. This equipment should not be used close to or stacked with other equipment.
Except for cables, connecting cables and other accessories sold by the manufacturer
as spare parts for internal components, the components cannot be replaced or repaired
without permission. Otherwise it may cause excessive electromagnetic interference or
disturbance.
❖ Do not use this device near strong radiation sources (such as unshielded RF sources)
as this may interfere with proper operation of the device.
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