Specifications - Sunrise Medical DeVilbiss RPM 9055 Serie Guía De Instrucciones

14

SPECIFICATIONS

Size .................................4.0"H x 7.5"W x 10.8"D (10.2 cm x 19.6 cm x 26.2 cm)
Weight....................................................................................3.8 lbs. (1.7 kg)
Electrical Requirements.............................100-240V~, 50/60 Hz or 120V~, 400 Hz
Maximum Power Consumption..........................65 watts max from AC power source
Bilevel CPAP Pressure Range ............................................................3-25 cmH
Pressure Delay Time ................................0 to 45 minutes, in 5 minute increments
Delay Pressure Range......................3 cmH
Operating Temperature Range.....................................41°F to 93°F (5°C to 34°C)
Operating Humidity Range ....................................0% to 95% RH non-condensing
Operating Atmospheric Conditions .....................................Sea level to 9,000 feet
Storage & Transportation Temperature Range. .......-40°F to 158°F (-40°C to +70°C)
Storage & Transportation Humidity Range................0% to 95% RH non-condensing
Maximum Limited Pressure.........................................30 cmH
Sound Level ......................................................................................< 30 dBA
Filter specs................................................Standard Filter > 3.0 micron particles
Max flow rates
83 L/m ...............................................................@ 8 cmH
134 L/m ............................................................@ 17 cmH
163 L/m ..................................................................@ 25 cmH
Pressure Accuracy ...........................................................................± 0.5 cmH
Pressure Swings (cmH O peak to peak at 500mL tidal volume)
2
Breaths per minute
@ 8 cmH O
2
@ 17 cmH O
2
@ 25 cmH O
2
NOTE–For results of extreme testing of static and dynamic pressure regulation refer to
the Sunrise Medical web site (www.sunrisemedical.com).
Warranty.................................................................................Two-year limited
Equipment classification with respect to protection from electric shock........Class II
Degree of protection from electric shock................................Type BF Applied Part
Degree of protection against ingress of liquids.............................................None
Equipment not suitable for use in the presence of a flammable anaesthetic mixture
with air or with oxygen or nitrous oxide.
Mode of operation ...........................................................................Continuous
Clinical Specifications for Digital Outputs
Mask Pressure..................................................................0 to 25.5 cmH
Patient Flow............................................................-127 to +127 L/min ± 10 L/min
Leak Flow.....................................................................................0 to +127 L/min
Estimated Tidal Volume ......................................................................0 to 1023 mL
NOTE–Leak and Tidal Volume are estimates. They are provided for trending purposes only.
SE-9055
O to EPAP or CPAP prescription pressure
2
Optional Fine Particle Filter > 0.3 micron particles
2
2
10 15 20
0.5 0.5 0.5
1.0 1.0 1.0
1.0 1.0 1.0
O
2
O under normal use
2
O (1/3 max pressure)
O (2/3 max pressure)
O (max pressure)
2
O
2
O ± 0.5
2
S p e c i f i c a t i o n s