Instructions For Use – neXus Ultrasonic Surgical Aspirator
Doc #: 100-10-1000 rev A
p 5
Electromagnetic Compatibility Guidance (in accordance with EN/IEC 60601-1-2:2014)
Table 1.1 Guidance & manufacturer’s declaration on electromagnetic emissions (EN table 201)
Note:
The emissions characteristics of this equipment make it suitable for use in industrial areas and hospitals. If it is used
in a residential environment (for which CISPR 11 class B is normally required) this equipment might not offer adequate
protection to radio-frequency communication services. The user might need to take mitigation measures, such as
relocating or re-orienting the equipment.
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
(Table 201)
The neXus Ultrasonic Surgical Aspirator System is intended for use in the electromagnetic environment specified below.
The customer or the user of neXus Ultrasonic Surgical Aspirator System should ensure that it is used in such an
environment.
Emissions test
Compliance
Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1
The neXus Ultrasonic Surgical Aspirator System uses RF energy only
for its internal function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby electronic
equipment.
RF emissions
CISPR 11
Class A
The neXus Ultrasonic Surgical Aspirator System is suitable for
use in all establishments other than domestic 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
Class A
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Complies
