Abbott 3599, Руководство для клиницистов

Страница: 47 / 60

CAUTION:
▪
The device complies with the limits for medical devices contained in IEC 60601-1-2:2014-04,
▪
CISPR11:2015 (BS EN 55011:2016), and ETSI EN 300 328 V2.1.1 (2016 ‑ 11). However, the device may
cause radio interference or may disrupt the operation of nearby equipment. It may be necessary to
mitigate this effect by reorienting or relocating the receiving device.
▪
To avoid increasing emissions or decreasing immunity from a device or system, use only components
▪
approved by Abbott Medical with this system. Do not use Abbott Medical components with devices or
systems that are not approved by Abbott Medical.
Table 7. Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
Emissions Test Compliance Electromagnetic Environment Guidance
RF emissions
CISPR 11
Group 1 The device produces RF emissions as a result of its internal and system interface functions. Its
RF emissions are very low and are not likely to cause any interference in nearby electronic
equipment.
RF emissions
CISPR 11
Class B The device is suitable for use in all establishments including domestic establishments and
those directly connected to the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/ flicker
emissions
IEC 61000-3-3
Not applicable
41
▪
▪