2-5
Important User Information Operator Manual 150832-639
2.5 Technical
Specifications
See Figure 2-4 through Figure 2-6.
2.5.1 Overall Size (W x L x H) • 22" wide x 81" long x 26 to 45" high*
(550 mm wide x 2055 mm long x 675 to 1136 mm high)
2.5.2 Range of Motion Height: 26 to 45" (675 to 1136 mm)*
Trendelenburg Range: 30° ±1°
Reverse Trendelenburg Range: 30° ±1°
Lateral Tilt Range: 20° ±1°
Slide Motion: HEAD: 9" (227 mm)*
FOOT: 9" (227 mm)*
Back Section Motion: UP: 80° ±1°
DOWN: 40° ±1°
Leg Motion: UP: 0°
DOWN: 105° ±1°
Kidney Elevator Mechanism: 4" (110 mm)*
Flex/Reflex: 140° ±1° / 100° ±1°
Head Motion (Manual): 90° ±1°
2.5.3 EMC Note the following:
• Medical Electrical Equipment needs special precautions
regarding EMC and needs installed and put into service
according to the EMC information provided in this manual.
• Portable and mobile RF communications equipment can affect
Medical Electrical Equipment.
• For table control via e-Serve (RS-232) connection, note the table
has been tested for EMC compliance using a 6’ (2 m) long,
shielded serial cable. A longer or unshielded cable could cause
problems and must be observed to verify normal operation.
• The use of accessories, transducers and cables other than those
specified by the manufacturer, may result in increased emissions
or decreased immunity of the STERIS 4085 General Surgical
Table.
• The STERIS 4085 General Surgical Table should not be used
adjacent to or stacked with other equipment. If so, table should be
observed to verify normal operation.
WARNING – PERSONAL
INJURY AND/OR EQUIPMENT
DAMAGE HAZARD: Use of
accessories, transducers or
cables with this table, other
than those specified, may result
in increased emissions or
decreased immunity of the
table.
CAUTION – POSSIBLE
EQUIPMENT DAMAGE:
Appropriate components of this
surgical table have been tested
and found in compliance with
IEC 60601-1-2:2001, Medical
Electrical Equipment – Part 1;
General Requirements for
Safety; Electromagnetic
Compatibility (EMC). There is,
however, a potential for
electromagnetic or other
interference between this
equipment and other devices.
Should user experience
interference, relocate this
device or minimize the use of
the affected equipment while
this device is in operation.
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