DeVilbiss CPAP Serie Manual Del Usuario página 14

Dispositivo de presión positiva en las vías respiratorias
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Dynamic Short-Term pressure accuracy with and without DV5HH Humidifier (per
iSO 17510-1:2007)
Waveform
Volume [mL]
Sinusoidal
cycle with I:E =
1:1
Maximum Flow-Rate (per iSO 17510-1:2007)
Measured pressure at the patient
connection port (cmH
O)
2
Average flow at the patient connection port
(l/min)
Long Term Static Pressure Accuracy ................................................................................................................. +/- 0.5 cmH
additional Specifications
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 ......................................................................................IPXI Drip-proof vertical
Mode of operation .................................................................................................................................................... Continuous
Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide
DEViLbiSS GuiDaNCE aND MaNuFaCTuRER'S DECLaRaTiON
WaRNiNG
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into
service according to the Electromagnetic Compatibility [EMC] information provided in the accompanying
documents.
Portable and Mobile RF Communications Equipment can affect Medical Electrical Equipment.
The equipment or system should not be used adjacent to or stacked with other equipment and that if adjacent or
stacked use is necessary, the equipment or system should be observed to verify normal operation in the
configuration in which it will be used.
NOTE– The EMC tables and other guidelines provide information to the customer or user that is essential in determining
the suitability of the Equipment or System for the Electromagnetic Environment of use, and in managing the
Electromagnetic Environment of use to permit the Equipment or System to perform its intended use without disturbing
other Equipment and Systems or non-medical electrical equipment.
EN - 14
Breath Rate [min-1]
500
10, 15, 20
3.0 cmH
Set Pressure
[cmH
3.0
9.0
14.0
20.0
25.0
Test Pressures
O
9.0 cmH
O
2
2
3.0
8.4
85.0
150.3
Pressure Accuracy
O]
[Pk-Pk cmH
2
14.0 cmH
O
20.0 cmH
2
13.0
19.1
154.0
150.6
O]
2
0.5
0.5
1.0
1.0
1.0
O
25.0 cmH
O
2
2
24.0
132.9
O
2
SE-DV56-1

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