Esaote MyLab XPro75, Начало работы

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A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y
MyLab
- G E T T I N G S T A R T E D 2 - 4

powering the ultrasound system from an outlet different
from the one of the interfering device,

contacting Esaote Service personnel for help.
Electro-Surgical Devices (ESUs)
Electro-surgical devices or other devices that introduce radiofrequency
electromagnetic fields or currents into the patient may interfere with the ultrasound
image. An electro-surgical device in use during ultrasound imaging will grossly
affect the 2D image and render Doppler modalities useless.
NOTE
Cables and accessories other than the supplied ones could negatively affect
EMC performance of the device.
Electromagnetic Emissions
NOTE
The EMISSIONS characteristics of this equipment make it suitable for use
in industrial areas and hospitals (CISPR 11 class A). 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
MyLab is suitable for use in the specified electromagnetic environment.
The purchaser or user of MyLab should assure that it is used in an electromagnetic
environment as described below:
Emission Test Compliance Electromagnetic Environment
RF emissions
CISPR 11
Group 1 This MyLab uses RF energy only for its
internal function. Therefore, the RF
emission is very low and not likely to cause
any interference in nearby electronic
equipment.
RF emissions
CISPR 11
Class A
MyLab
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
Complies
Class A
Voltage fluctuations
and flicker emissions
IEC 61000-3-3
Complies