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Vers. 20210510ENG Page 31
SECTION 8: EXPLANATION AND RISK WARNING ON
EMC
8.1 Explanation and Risk Warning on EMC
This product has passed the EMC test and meets GB/T 18268.1–2010 "Electromagnetic
compatibility requirements for electrical equipment for measurement, control and laboratory
use - Part 1: General requirements" and GB/T 18268.26–2010 "Measurement, control and
laboratory Electromagnetic compatibility requirements for electrical equipment - Part 26:
Particular requirements for in vitro diagnostic (IVD) medical devices.
The following usage requirements should be strictly observed during use, otherwise it may
cause electromagnetic interference to other equipment or reduce the anti-electromagnetic
interference capability of this product, or even lose its basic performance.
This product belongs to Group 1 Class A equipment of GB 4824–2013 and is suitable for use
in all facilities that are not directly connected to the public low-voltage power grid of the
residential home.
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 product, and portable and mobile RF communications equipment
should be guaranteed to meet certain spatial distances and specific requirements. See the
requirements in Table 4.
If the equipment cable connection is faulty, please contact our company for repair or
replacement, otherwise it may cause excessive electromagnetic interference. If the
equipment is faulty, please contact scil’s Technical Support Services. Do not repair or
replace the components yourself, otherwise it may cause excessive electromagnetic
interference.
In addition to the transducers and cables sold by the manufacturer of the equipment or
system as spare parts for internal components, the use of accessories, transducers and
cables outside the specified regulations may lead to increased emission or reduced immunity
of equipment or systems.
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