The NeoBip is a Bilevel positive airway pressure unit.It is intended for
the treatment of obstructive sleep apnea (OSA) for adult or pulmonary
Insufficiency who need respiratory support.The device is intended for
home,hospital and other institutional environment use.
This device is not intended for life support.
The device is to be used only on the instruction of a licensed health
care professional who has received operation training from the
company or other authorized organzations. Pressure settings should be
determined with the configuration of the device according to your health
care professional’s prescription.


• 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.

Benefits & Specifications

• AEONMED NeoBip BiPAP Device Non Invasive Ventilator
• Its Tidal Volume 50-2000 ML
• Ventilation modes: CPAP, AUTOS, S, T, S/T, VGPS
• Therapy Modes: CPAP, S, ST, T, VGPS
 CPAP: Continuous Positive Airway Pressure mode, suitable for Obstructive Sleep Apnea.
 AUTOS: Intelligent regulation of inspiratory pressure to ensure a more smooth and comfortable breath.
 S: Spontaneous ventilation mode, suitable for patients with spontaneous respiratory.
 T: Timed mode, suitable for patients without spontaneous respiratory capacity.
 S/T: The machine automatically switches between S and T modes according to patient's respiratory condition.
 VGPS: Volume Guarantee Pressure Support, meets patient's tidal volume requirement with its minimum pressure.
• Device Non-Invasive Ventilator. Accurate intelligent control for every comfortable breath.
• Intended for the treatment of Obstructive Sleep Apnea for the adults or pulmonary insufficiency patients
who need respiratory support.
• VGPS (Volume Guarantee Pressure Support) mode, ensures the ventilation volume target.


Device Size

Dimensions: 160 mm × 148 mm × 99.5 mm, or 247 mm × 148mm × 99.5 mm (with the humidifier)


 0.82 kg, or 1.26 kg (with the humidifier)

Operation, Transport and Storage

Operation Transport and Storage Temperature 5℃ to 35℃ -20℃ to +60℃ Humidity 10% to 93% Noncondensing 10% to 93% Noncondensing Atmospheric Pressure 760 to 1060 hPa 500 to 1060 hPa

Mode of Operation




SD Card

With a capacity≥8G, the SD card can record patient data and fault information.

AC Power adapter

Input: 100-240VAC, 50-60 Hz, 2.0 A max Output: 24Vdc, 3.33A

Main Device

Input: 24Vdc, 3.33A max

Type of Protection Against Electric Shock

Class II Equipment

Degree of Protection Against Electric Shock

Type BF Applied Part

Degree of Ingress Protection


Pressure Range

AUTOS, ST, T, VGPS: 4 to 30 cm H2O (4 to 30 hPa) CPAP : 4 to 20 cm H2O (4 to 20 hPa) ≤40 hPa under single fault conditions

Ramp time

The ramp time ranges from 0 to 60 minutes

Sound Pressure Level

<30 dBA, when the device is working at the pressure of 10 hPa.

Sound Power Level

<38 dBA, when the device is working at the pressure of 10 hPa.

Measurement system uncertainties

In accordance with ISO 80601-2-70:2015 the measurement uncertainty of the manufacturer's test equipment is: For measures of flow ± 2% of the reading or 0.05Std L/min(whichever is greater) For measures of pressure ±0.5%for full scale(15.6-25.6℃),± 1.5%for full scale(0-15.6℃15.6-40℃)

Pressure Accuracy

 Maximum static pressure variation at 10 cm H2O (10 hPa)

Maximum Flow

Test Pressure(hPa) 4 8 12 16 20 Average Flow at the Patient Connection Port(l/min) 91 111 120 131 123


Length: 1.8m Inner diameter: 19mm


Range: 70%-100%. Accuracy: ±3%.

Pluse Rate

Range: 20-250BPM. Accuracy: ±3digits

Wireless module

Frequency range: 2,402-2,480 MHz Maximum output power: +4.0dbm Modulation: GFSK

Wireless module

Frequency range: 2,412-2,484 MHz Maximum output power: +20.0dbm Modulation: CCK, OFDM


The bias error and the linearity error have been considered in above pressure variation


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