+91 9115 300 300-
business@hitwinhealthcare.com
+91 9115 300 300 business@hitwinhealthcare.com
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• BPAP System (Y Series) is a Bi-level PAP (Bi-level Positive Airway Pressure) device, which is intended to provide non-invasive ventilation for patients with obstructive Sleep Apnea (OSA) and Respiratory Insufficiency.
• These devices are intended for adult patient by prescription in the home or hospital/institutional environment. This device is not intended for life support.
• The optional Heated Humidifier used with the Y Series together is indicated for taking humidifying and heating air from the device. The optional SpO2 module used with the Y Series together is indicated for monitoring the patient's SpO2 and pulse rate auxiliarily.
• A BIPAP is a Non invasive therapy it a pressure controlled in a spontaneous breathing. • It is used to help you breathe easier when you have condition that make breathing difficult . • Obstructive sleep apnea is a serious condition in which your breathing stop and starts repeatedly while you are asleep. • Chronic obstructive pulmonary disease (copd) • Asthma • Obesity hypoventilation syndrome. • Heart condition such as congestive heart failure or coronary artery disease • A neurological or neuromuscular disorder that affect your ability to breathe. • Poor breathing after a medical procedure such as surgery. • The machine works by pushing the pressurized air into your lungs. • It reduces burden on respiratory muscles and lungs to inhale and exhale • The machine motor blows air through the tube certain amount of required pressure. • The pressurized air enters your body through the mask or plugs. • It eliminates need for using a ventilator that makes uses of a tube that goes down into your throat without used for tracheotomy. • A tracheotomy is a procedure to create a hole in your neck to let you breathe through the trachea.
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Device Size |
Dimensions:
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170 mm × 180 mm × 118 mm, or 290 mm × 180 mm × 134 mm (with the humidifier) |
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Weight: |
1.5 kg, or 2.5 kg (with the humidifier) |
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Product Use, Transport and Storage |
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Operation |
Transport and Storage |
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Temperature: 5° C to 35° C (41˚F to 95˚F) |
-25° C to 70° C (-13˚F to 158˚F) |
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Humidity: 15% to 93% Non-condensing |
15% to 93% Non-condensing |
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Atmospheric Pressure: 760 ～ 1060 hPa |
760 ～ 1060 hPa |
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Mode of Operation |
Continuous |
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Work Mode |
CPAP, S, AutoS, Auto CPAP, S/T, T |
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SD Card |
SD card can record patient data and fault information. |
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AC Power Consumption |
100 - 240 V ～, 50 / 60 Hz, 2- 1 A. |
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Main Device offer to USB Communications Port |
5 V ～ 2.0 A |
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Main Device offer to Humidifier |
24 V ～ 1.5 A |
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Electric Shock |
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Type of Protection Against Electric Shock |
Class II Equipment |
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Degree of Protection Against Electric Shock |
Type BF Applied Part |
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Degree of Protection Against Ingress of Water |
IP22 |
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Pressure Range |
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IPAP |
4.0 ～ 30.0 hPa ; in 0.5 hPa increments. |
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EPAP |
4.0 ～ 25.0 hPa ; in 0.5 hPa increments. |
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CPAP mode: |
4.0 ～ 20.0 hPa |
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Under single fault conditions,
≤ 30 hPa for CPAP mode,
≤ 40 hPa for the rest modes.
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Pressure Display Accuracy |
± (0.8 hPa＋4%) |
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Static Pressure Stability |
± 0.5 hPa |
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Ramp |
The ramp time ranges from 0 to 60 minutes. |
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Sound Pressure Level |
＜30 dB, when the device is working at the pressure of 10 hPa. |
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Sound Power Level |
＜38 dB, when the device is working at the pressure of 10 hPa. |
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Maximum Flow |
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Test Pressure (hPa) |
4 |
9 |
15 |
20 |
25 |
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Measured Pressure at the Patient Connection Port (hPa) |
3 |
8 |
14 |
19 |
24 |
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Average Flow at the Patient Connection Port (l/min) |
93.2 |
97.6 |
98.1 |
98.5 |
99.1 |
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SpO2 Range: |
0% ～ 100% The margin of error for SpO2 between 70% and 100% is ± 3%.
No strict accuracy requirements for SpO2 below 70%. |
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Pulse Rate |
Range: 40 ～ 240 BPM |
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Margin of Error: ± 1% |
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Wavelengths |
Red: 663 nanometers Infrared: 890 nanometers |
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Maximal Optical Output Power |
Less than 1.5 mw maximum average. |
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Tube |
Length: 6 ft. (1.83 m) |
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The Form and the Dimensions of the Patient Connection Port |
The 22 mm conical air outlet complies with ISO 5356-1. |
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