User's Manual Part 3

10-30
G. Manufactures Technical Declaration
EMC Information Tables as required by EN 60601-1-2:2007 Clause 5
In accordance with EN 60601-1-2:2007 Medical Electrical Equipment Part 1-2: General
requirements for safety Collateral standard: Electromagnetic Compatibility Requirements and
tests
1. “Medical Electrical Equipment needs special precautions regarding EMC and needs
to be installed and put into service according to the EMC information provided in the
Accompanying Documents” (the following tables).
2. Portable and Mobile RF Communications Equipment can affect Medical
Electrical Equipment”.
3. “The equipment or system should not be used adjacent to or stacked with other
equipment and that if adjacent or stacked use is necessary, the equipment or system
should be observed to verify normal operation in the configuration in which it is used”.
The following tables (as required in EN 60601-1-2:2007) provide information regarding the
Electromagnetic Compatibility (EMC) of this product and its accessories.
Table 201Guidance and manufacturer’s declarationelectromagnetic emissionsfor all
EQUIPMENT and SYSTEMS
Guidance and manufacturer’s declarationelectromagnetic emissions
The 3880 System is intended for use in the electromagnetic environment specified below.
The customer or the user of the 3880 System should assure that it is used in such an
Emissions Test
Compliance
Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1
The 3880 System must emit electromagnetic
energy in order to perform its intended function
(remote communications within an specific band for
WLAN; i.e. 2.431 to 2.474 GHz).
Nearby electronic equipment may be affected.
RF emissions
CISPR 11
Class B
The 3880 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
Not applicable
Voltage
fluctuations/flicker
emissions IEC
61000-3-3
Not applicable