Verathon GLIDESCOPE GO Operation & Maintenance Manual page 28

Table 4. Guidance and Manufacturer's Declaration —Electromagnetic Immunity
The system is intended for use in the electromagnetic environment specified below. The customer or the
user of the system should ensure that it is used in such an environment.
Immunity Tests
Radiated
RF: hospital
environment
IEC 61000-4-3
Radiated RF:
home healthcare
environment
IEC 61000-4-3
Note: U is the AC mains voltage prior to application of the test level.
T
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
ELECTROMAGNETIC EMISSIONS
Table 5. Guidance and Manufacturer's Declaration—Electromagnetic Emissions
The system is intended for use in the electromagnetic environment specified below. The customer or
the user of the system should ensure that it is used in such an environment.
Emissions Test
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/flicker emissions
IEC 61000-3-3
ACCESSORY CONFORMANCE TO STANDARDS
To maintain electromagnetic interference (EMI) within certified limits, the system must be
used with the cables, components, and accessories specified or supplied by Verathon. For
additional information, see
other than those specified or supplied may result in increased emissions or decreased
immunity of the system.
Table 6. EMC Standards for Accessories
Accessory
Monitor power adapter
Charging cradle power adapter
22
0900-4788 REV-10
IEC 60601 Test Level
3 V/m
80 MHz–2.7 GHz
80% AM at 1 kHz
10 V/m
80 MHz–2.7 GHz
80% AM at 1 kHz
Compliance
Group 1
compliance
System Parts &
Compliance Electromagnetic Environment –
Level
Interference may occur in the vicinity
of equipment marked with the
following symbol:
In compliance
Electromagnetic Environment – Guidance
The 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.
Class B
The system is suitable for use in home
Class B healthcare and professional hospital
environments.
In
Accessories. The use of accessories or cables
Max Cable Length
Guidance
1.5 m (4.9 ft)
1.5 m (4.9 ft)