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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.
Target Tidal Volume
Pressure support automatically adjusts according to target tidal volume as to improve hypoventilation. Real time monitoring includes Pressure, Flow, Expiratory tidal volume (Vte), Respiratory rate (RR), Minute ventilation (MV), Leak, Inspiration time (Ti), SpO2* and Pulse rate (PR)*.
Ventilation efficacy
Advanced leakage compensation promises adequate volume support. Ti Control, I/E Sense and Rise time guarantee better ventilation synchronization.
Other key features
· BMC+ iCode App
· SpO2 Kit (Optional)
· GPRS / Wi-Fi Kit (Optional, individually or combined with SpO2 Kit)
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) Humidity: 15% to 93% Non-condensing Atmospheric Pressure: 760 to 1060 hPa |
-25°C to 70°C (-13˚F to 158˚F) 15% to 93% Non-condensing 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.
Regarding any queries.