The RESmart GII BPAP System represents a breakthrough in sleep therapy technology, designed to provide advanced treatment for individuals suffering from sleep-related breathing disorders. This innovative system offers a range of features and capabilities aimed at improving comfort, efficacy, and ease of use for both patients and healthcare providers.

An intelligent technology, featured in the RESmart GII Y/U series, it delivers automatic solution for patients with OSA and/or respiratory insufficiency. Aligned with same platform as RESmart GII BPAP System, Y series adapt pressure automatically to patient’s needs and provide a better synchronization.

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 to 1060 hPa 760 to 1060 hPa
Mode of Operation
Continuous
Work Mode
CPAP, S, AutoS, AutoCPAP, S/T, T
SD Card
SD card can record patient data and fault information.
AC Power Consumption
100 – 240 V ～ 2 – 1 A, 50 / 60 Hz
Main Device offer to USB Communications Port
5 V 2.0 A
Main Device offer to Humidifier
24 V 1.5 A
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 ～ 20.0 hPa (only applies to Y-20T, U-20T); 4.0 ～ 25.0 hPa (only applies to Y-25T,
U-25T); 4.0 ～ 30.0 hPa (only applies to Y-30T, U-30T, U-30AT); in 0.5 hPa increments.
EPAP: 4.0 ～ 20.0 hPa (only applies to Y-20T, U-20T); 4.0 ～ 25.0 hPa (only applies to
Y-25T, Y-30T, U-25T, U-30T, U-30AT); 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.