Abbott 3599 - Electromagnetic Emissions Guidance; RF Emissions Guidance

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 operaon of nearby equipment. It may be necessary to
migate this eect by reorienng or relocang the receiving device.
▪ To avoid increasing emissions or decreasing immunity from a device or system, use only components▪
approved by Abbo Medical with this system. Do not use Abbo Medical components with devices or
systems that are not approved by Abbo Medical.
Table 7. Guidance and Manufacturer’s Declaraon – Electromagnec Emissions
Emissions Test Compliance Electromagnec Environment Guidance
RF emissions
CISPR 11
Group 1 The device produces RF emissions as a result of its internal and system interface funcons. 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 domesc establishments and
those directly connected to the public low-voltage power supply network that supplies
buildings used for domesc purposes.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage uctuaons/ icker
emissions
IEC 61000-3-3
Not applicable
41
▪
▪