Table 10. Technical specicaons
Output voltage 5 VDC
Output current up to 1 A
Power adapter
cercaon marking
Power adapter should have one or more of the following
cercaon markings:
Appendix D: Electromagnec Compability
Guidelines
The charging system (Model 16000), hereaer the device, is medical equipment and
should be used with the following guidance.
The device requires special precauons with regard to electromagnec compability
(EMC) and should be used in accordance with the informaon provided in this manual.
The device has essenal performance, as dened by
IEC 60601‑1:2005+AMD1:2012+AMD2:2020 (Ed 3.2). Performance of the device was
maintained during electromagnec disturbance tesng.
The device is intended for use in the electromagnec environment specied in the
following tables. The user should ensure that it is used in such an environment.
CAUTION:
▪ The device complies with the limits for medical devices contained in▪
IEC 60601‑1‑2:2014+AMD1:2020 (Ed 4.1) and
CISPR11:2015+AMD1:2016+AMD2:2019 (BS EN 55011:2016+A2:2021). However,
the device may cause radio interference or may disrupt the operaon of nearby
equipment. It may be necessary to migate this eect by reorienng or
relocang 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 11. Guidance and Manufacturer's Declaraon - Electromagnec Emissions
Emissions Test Compliance Electromagnec Environment
Guidance
RF emissions
CISPR 11
Group 1 The device produces RF emissions as
a result of its internal and system
interface funcons. 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 domesc
establishments and those directly
connected to the public low-voltage
Harmonic emissions IEC 61000-3-2 Class A*
23
▪
▪