Important Safety Information
Regulatory
xiv Service Manual
Beginning in September 2016, some medical devices sold in the USA must be labeled with a Unique Device
Identifier (UDI). The UDI label will be located on or adjacent to the serial number label on the device.
Example of UDI label format:
Regulatory
GE Healthcare has declared that this product conforms with the European Council Directive 93/42/EEC
Medical Device Directive when it is used in accordance with the instructions provided in the Operation and
Maintenance Manual.
Standards
This device is designed to meet the requirements of:
• IEC 60601-2-21 with amendment
• IEC 60601-1 with amendment
• IEC 60601-1-2 with amendment
• UL 60601-1
• BSEN - 45501 with amendment
This symbol indicates that the waste of electrical and electronic equipment
must not be disposed as an unsorted municipal waste and must be collected
separately. Please contact an authorized representative of the manufacturer
for information concerning the decommissioning of your equipment.
Equipment shall be used only by qualified, trained medical personnel.
Do not step or stand on surface.
Acceptable mattress height range.
Symbol Description
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