GE Transport Pro, Руководство по обслуживанию

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2-2 Transport Pro Revision A
2012659-042
Equipment Overview: General
General
Safety Information
Manufacturer’s Responsibility
GE is responsible for the effects of safety, reliability, and performance
only if:
„
Assembly operations, extensions, readjustments, modifications, or
repairs are carried out by persons authorized by GE.
„
The electrical installation of the relevant room complies with the
requirements of the appropriate regulations.
„
The equipment is used in accordance with the instructions for use.
Classification Information
EN
This device is intended for use under the direct supervision of a licensed
health care practitioner.
This device is not intended for home use.
Federal law restricts this device to be sold by or on the order of a
physician.
Contact GE for information before connecting any devices to the
equipment that are not recommended in this manual.
Parts and accessories used must meet the requirements of the applicable
EN 60601 series safety standards, and/or the system configuration must
meet the requirements of the EN 60601-1-1 medical electrical systems
standard.
Periodically, and whenever the integrity of the device is in doubt, test all
functions.
The use of ACCESSORY equipment not complying with the equivalent
safety requirements of this equipment may lead to a reduced level of
safety of the resulting system. Consideration relating to the choice shall
include:
„
use of the accessory in the PATIENT VICINITY; and
„
evidence that the safety certification of the ACCESSORY has been
performed in accordance to the appropriate EN 60601-1 and/or EN
60601-1-1 harmonized national standard.
If the installation of the equipment, in the USA, will use 240 V rather
than 120 V, the source must be a center-tapped, 240 V, single-phase
circuit.