Introduction
2067634-077 Revision B
SEER™ 1000
19
Supply and Accessory Information
For ordering information and a list of supplies and accessories that have
been approved for use with this device, see the
SEER 1000 Supplies and
Accessories Reference Manual
that is supplied with each recorder.
Manufacturer Responsibility
The manufacturer is responsible for the effects of safety, reliability, and
performance only if the following conditions are met:
Assembly operations, extensions, readjustments, modifications, or re-
pairs are carried out by persons authorized by GE Healthcare.
The electrical installation of the relevant room complies with the re-
quirements of the appropriate local, state, and other government reg-
ulations.
The equipment is used in accordance with the instructions for use.
GE Healthcare is contacted for information before any devices that
are not recommended in this manual are connected to the equip-
ment.
Product and Package Information
This section describes the location of the labels used on your device and
its packaging. It also describes the symbols used on the labels.
Symbols
The following symbols may appear on the device or its packaging. Famili-
arity with these symbols assists in the safe use and disposal of the equip-
ment. For equipment symbols not shown, refer to the original equipment
manufacturers (OEM) manuals.
Symbols are used to convey warnings, cautions, prohibitions, mandatory
actions, or information. Any hazard symbol on your device or packaging
with markings in color indicates there is certain danger and is a warning.
Any hazard symbol on your device or packaging that is in black and white
indicates a potential hazard and is a caution.
