EndoShield 2
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Technical Specifi cations (continued)
Standards and IEC Classifi cations
Internally Powered Equipment per IEC 60601-1/EN 60601-1
Equipment operates from an internal electrical power source.
Defi brillator Protected Equipment
The electrosurgical generator provides defi brillator protection. The Endoshield 2
does not compromise this protection.
Caution:
Ordinary equipment is not protected against the ingress of water.
Caution:
Medical Electrical Equipment needs special precautions regarding
electromagnetic compatibility (EMC) and needs to be installed and put into service
according to the EMC information provided herein.
Caution:
Portable and mobile RF communications equipment can aff ect Medical
Electrical Equipment.
Electromagnetic emissions and immunity per IEC 60601-1-2/EN 60601-1-2
Guidance and Manufacturer’s Declaration
–
Emissions
The EndoShield 2 is intended for use in the electromagnetic environment specifi ed below. The
customer or user of the EndoShield 2 should ensure that it is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment
–
Guidance
RF emissions
CISPR 11
Group 1
The EndoShield 2 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 B
The EndoShield 2 is suitable for use in all
establishments, including domestic, and those
directly connected to the public low-voltage
power supply network that supplies buildings
used for domestic purposes.
Harmonics
IEC 61000-3-2
N/A
Flicker
IEC 61000-3-3
N/A