EN
Medical electrical equipment
Part 1: General requirements for safety
EN 60601-1-1 (IEC 60601-1-1)
Medical electrical equipment
Part
Collateral standard: Safety requirements for Medical electrical systems
EN 60601-1-2 (IEC 60601-1-2)
Medical electrical equipment
Part
Collateral standard: Electromagnetic compatibility; Requirements and tests
Accessory equipment connected to the analog and digital interfaces must be in com- pliance with the respective nationally harmonized IEC standards (i.e. IEC 60950 for data processing equipment, IEC 60065 for video equipment, IEC
FCC Class B
This equipment has been tested and found to comply with the limits for a Class B dig- ital device, pursuant to Part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against harmful interfer- ence when the equipment is operated in a residential environment. This equipment generates, uses, and can radiate radio frequency energy. If not installed and used in accordance with this user's manual, it may cause harmful interference to radio com- munications.
Note that even when this equipment is installed and used in accordance with this user's manual, there is still no guarantee that interference will not occur. If this equip- ment is believed to be causing harmful interference to radio or television reception, this can be determined by turning the equipment on and off. If interference is occur- ring, the user is encouraged to try to correct the interference by one or more of the following measures:
!Reorient or relocate the receiving antenna.
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