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Y30T

Overview

• 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.

Description

• 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

• 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

Specifications

-

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.

Video

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