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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.
Categories: BILEVEL, BILEVEL / NIV/ BPAP
• 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.
• CPAP, S, S / T, T operating modes
• IPAP 4-30 cm H2O,
• EPAP 4-30 cm H2O
• 8-step inhalation-exhalation triggers
• Adjusting the inhalation-exhalation pressure, inhalation time (0.5-3 seconds) and respiration rate
• 3.5 "colour LCD Screen; high-quality body and humidifier materials
• Monitoring Vt, Respiratory Rate, Min Vent, Leak. Alarms in all respects.
• 5-step adjustment of the humidifier
• Display of the key parameters of therapy in the online mode
• Build quality conforms to German standards
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| Device Size | Dimensions:
| 170 mm × 180 mm × 118 mm, or 290 mm × 180 mm × 134 mm (with the humidifier) | ||||
| Weight: | 1.5 kg, or 2.5 kg (with the humidifier) | |||||
| Product Use, Transport and Storage | ||||||
| Operation | Transport and Storage | |||||
| Temperature: 5° C to 35° C (41˚F to 95˚F) | -25° C to 70° C (-13˚F to 158˚F) | |||||
| Humidity: 15% to 93% Non-condensing | 15% to 93% Non-condensing | |||||
| Atmospheric Pressure: 760 ～ 1060 hPa | 760 ～ 1060 hPa | |||||
| Mode of Operation | Continuous | |||||
| Work Mode | CPAP, S, AutoS, Auto CPAP, S/T, T | |||||
| SD Card | SD card can record patient data and fault information. | |||||
| AC Power Consumption | 100 - 240 V ～, 50 / 60 Hz, 2- 1 A. | |||||
| Main Device offer to USB Communications Port | 5 V ～ 2.0 A | |||||
| Main Device offer to Humidifier | 24 V ～ 1.5 A | |||||
| Electric Shock | ||||||
| Type of Protection Against Electric Shock | Class II Equipment | |||||
| Degree of Protection Against Electric Shock | Type BF Applied Part | |||||
| Degree of Protection Against Ingress of Water | IP22 | |||||
| Pressure Range | ||||||
| IPAP | 4.0 ～ 30.0 hPa ; in 0.5 hPa increments. | |||||
| EPAP | 4.0 ～ 25.0 hPa ; in 0.5 hPa increments. | |||||
| CPAP mode: | 4.0 ～ 20.0 hPa | |||||
Under single fault conditions,
≤ 30 hPa for CPAP mode,
≤ 40 hPa for the rest modes.
| Pressure Display Accuracy | ± (0.8 hPa＋4%) | ||||
| Static Pressure Stability | ± 0.5 hPa | ||||
| Ramp | The ramp time ranges from 0 to 60 minutes. | ||||
| Sound Pressure Level | ＜30 dB, when the device is working at the pressure of 10 hPa. | ||||
| Sound Power Level | ＜38 dB, when the device is working at the pressure of 10 hPa. | ||||
| Maximum Flow | |||||
| Test Pressure (hPa) | 4 | 9 | 15 | 20 | 25 |
| Measured Pressure at the Patient Connection Port (hPa) | 3 | 8 | 14 | 19 | 24 |
Average Flow at the Patient Connection Port (l/min) | 93.2 | 97.6 | 98.1 | 98.5 | 99.1 |
| SpO2 Range: | 0% ～ 100% The margin of error for SpO2 between 70% and 100% is ± 3%.
No strict accuracy requirements for SpO2 below 70%. | ||||
| Pulse Rate | Range: 40 ～ 240 BPM | ||||
| Margin of Error: ± 1% | |||||
| Wavelengths | Red: 663 nanometers Infrared: 890 nanometers | ||||
| Maximal Optical Output Power | Less than 1.5 mw maximum average. | ||||
| Tube | Length: 6 ft. (1.83 m) | ||||
| The Form and the Dimensions of the Patient Connection Port | The 22 mm conical air outlet complies with ISO 5356-1. | ||||