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GII

Overview

• The E-20A system is a CPAP (Continuous Positive Airway Pressure) device designed for the treatment of adult Obstructive Sleep Apnea (OSA) only, either in the hospital or at home.
• The device is to be used only on the instruction of a licensed health care professional. Your home care provider will make the correct pressure settings according to your health care professional’s prescription.
• Several accessories are available to make your OSA treatment with this device as convenient and comfortable as possible. To ensure that you receive the safe, effective therapy prescribed for you, use only BMC accessories.

Description

• Continuous positive airway pressure (CPAP) is a method for patient who have sleep apnea disorders.obstructive sleep apnea is a sleep disorders when your breathing stop and starts. • Obstructive sleep apnea causes interruption breathing often because your throat or airway temporarily block them. • A CPAP machine works a compressor motor generates a continuous steam of pressurized air that travel through an air filter into a flexible tube. • The machine works on a steady floe of pressurized air into your nose and mouth as you sleep it keep your airways helps breathe normally. • The airstream from the CPAP machine pushes against any blockages opening your airways so your lungs receives plenty of oxygen. • It improves your ability to sleep without walking up. • It lowers your risk of having a heart attack stroke or other cardiovascular attack. • It hepls lower your blood pressure. • It reduces daytime sleepiness. • It may reduce blood glucose and cholesterol level. • Blood pressure • Heart disease • Reduce stroke risk • Upper airway resistance syndrome

Benefits & Specifications

• RESlex Pressure Relief
• Auto-Adjusting Technology & Sensitivity Setting
• iCode Advanced Data
• iPhone and Android Apps Available
• 365 Days of On-Board Memory
• Auto On-Off Feature
• Auto Altitude Compensation
• Power Off Alert
• Leak Alert
• Integrated Heated Humidifier Included
• Easy Carry Handle

Specifications

-

Name

Function

Humidifier Indicator

Indicate the humidity level. There are five levels in total. The number of indicator lights that light up is directly proportional to the humidity level. If none of the indicator lights light up, it means the humidifier is turned off

Mute Button

Press this button to mute the alert. However, if the problem causing the alert is not solved, the alert will sound again two minutes later

Knob

Start treatment and adjust device settings

Ramp Button

Enable the Ramp feature

Display Screen

Display menus for operation, messages, monitoring data, etc

Power Indicator

Indicate the power supply status

Air Outlet

Deliver pressurized air; connected to the tube or the air inlet of the humidifier

Humidifier Connector

Provide power to the humidifier which is connected to the main device

Shield

Connect the humidifier to the main device after this shied is removed

SD Card Slot

Insert the SD card into this slot

Communications Port

Connected to external equipment (Not for connection to the phone or computer)

DC Inlet

An inlet for the DC power supply

Filter Cap

Place the cap on the air filter, which is used to filter dust and pollen in the air entering the device

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

SD Card

The SD card can record patient data and fault information.

AC Power Consumption

100 ~ 240 V AC, 50 / 60 Hz, 2.0 A max

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

Pressure Range

4 to 20 hPa (in 0.5 hPa increments),

≤30 hPa under single fault conditions.

Pressure Display Accuracy

± (0.5 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

8

12

16

20

Measured Pressure at the Patient Connection Port (hPa)

3

7

11

15

19

Average Flow at the Patient

Connection Port (l/min)

80

92

91.5

91

96

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: ± 3%

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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