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• Lumis 150 ST is a non-invasive ventilator designed for non-dependent patients with respiratory insufficiency. • It includes unique volume assurance mode iVAPS (intelligent Volume Assured Pressure Support). • It maintains target alveolar ventilation to suit each patient's changing needs. • Optional AutoEPAP ensures adequate EPAP is delivered to maintain an open upper airway - automatically, while an intelligent Backup Rate (iBR) encourages spontaneous breathing. • It also easy to set up and use.
Categories: BILEVEL, BILEVEL / NIV/ BPAP
• 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.
• Individually responsive with Intelligent Air • Intelligent Air is a collection of ResMed technologies that can tailor therapy to individual breathing needs: • iVAPS learns each patient’s unique alveolar ventilation, sets appropriate targets, then provides smooth pressure support to suit. • intelligent Backup Rate (iBR) gives patients maximum opportunity to trigger the ventilator. Staying out of the way until needed, iBR adds backup breaths to comfortably bring patients back to target. *Available in iVAPS and ST modes. • AutoEPAP maintains upper airway patency by auto-adjusting the expiratory pressure in response to partial and full obstructions. Available in iVAPS mode. • Vsync provides excellent patient–ventilator synchrony, even in the presence of significant leak. • TiControl lets you set min and max limits on either side of the patient’s ideal inspiratory time to encourage spontaneous breathing. • Trigger and cycle helps you optimise settings according to the patient’s condition, using five trigger and cycle sensitivity levels. • QuickNav for low-touch therapy adjustment. By simply double-clicking the home button on the device, you can toggle between the Settings and Monitoring screens to change and check settings quickly and easily. • Climate Control Auto for automatic humidification. When used with a HumidAir™ heated humidifier and ClimateLineAir™ heated tube, Lumis delivers humidification automatically – no settings to change and no complicated menus to navigate. • Ramp and Ramp Down for extra comfort. Lumis offers both Ramp and Ramp Down features to help patients ease into and out of each therapy session. • ResScan software for advanced clinical insights. ResScan enables you to download your patients’ therapy data, change ventilator settings, and gain insight into their therapy progress across a number of metrics (including AHI, leak and pressure). High-resolution data (at 25 Hz) is also available for breath-by-breath analysis and even greater insight. • Climate Control Auto for automatic humidification. • IntelligentAir auto-adjusting therapy modes. • QuickNav for low touch therapy adjustments.
| power supply unit | AC input range: 100–240V, 50–60Hz 1.0–1.5A, Class II 115V, 400Hz 1.5A, Class II (nominal for aircraft use) DC output: 24V 3.75A Typical power consumption: 53W (57VA) Peak power consumption: 104W (108VA) |
| Environmental conditions | Operating temperature: +41°F to +95°F (+5°C to +35°C) Note: The air flow for breathing produced by this therapy device can be higher than the temperature of the room. Under extreme ambient temperature conditions (104°F/40°C) the device remains safe. Operating humidity: 10 to 95% relative humidity, non-condensing Operating altitude: Sea level to 8,500' (2,591 m); air pressure range 1013 hPa to 738 hPa Storage and transport temperature: -4°F to +140°F (-20°C to +60°C) Storage and transport humidity: 5 to 95% relative humidity, non-condensing |
| Electromagnetic compatibility | The AirCurve 10 complies with all applicable electromagnetic compatibility requirements (EMC) according to IEC 60601-1- 2:2014, for residential, commercial and light industry environments. It is recommended that mobile communication devices are kept at least 1 m away from the device |
| Sensors | Pressure sensor: Internally located at device outlet, analog gauge pressure type, 0 to 40 cm H2O (0 to 40 hPa) Flow sensor: Internally located at device inlet, digital mass flow type, -70 to +180 L/min |
| Maximum single fault steady pressure | Device will shut down in the presence of a single fault if the steady state pressure exceeds: 30 cm H2O (30 hPa) for more than 6 sec or 40 cm H2O (40 hPa) for more than 1 sec |
| Sound | Pressure level measured according to ISO 80601-2-70:2015 (CPAP mode): SlimLine: 25 dBA with uncertainty of 2 dBA Standard: 25 dBA with uncertainty of 2 dBA SlimLine or Standard and humidification: 27 dBA with uncertainty of 2 dBA Power level measured according to ISO 80601-2-70:2015 (CPAP mode): SlimLine: 33 dBA with uncertainty of 2 dBA Standard: 33 dBA with uncertainty of 2 dBA SlimLine or Standard and humidification: 35 dBA with uncertainty of 2 dBA |
| Dimensions (H x W x D) | 4.57" x 10.04" x 5.91" (116 mm x 255 mm x 150 mm) |
| Temperature | Maximum heater plate: 154°F (68°C) Cut-out: 165°F (74°C) Maximum gas temperature: ≤ 106°F (≤ 41°C) |
| Air filter | Standard: Material: Polyester non woven fiber Average arrestance: >75% for ~7 micron dust Hypoallergenic: Material: Acrylic and polypropylene fibers in a polypropylene carrier Efficiency: >98% for ~7-8 micron dust; >80% for ~0.5 micron dust |
| Operating pressure range | S, ST, T: 3 to 25 cm H2O (3 to 25 hPa) VAuto: 4 to 25 cm H2O (4 to 25 hPa) CPAP: 4 to 20 cm H2O (4 to 20 hPa) |
| Supplemental oxygen Maximum flow: | For VAuto device: 4 L/min (CPAP, S, VAuto) For S device: 4L/min (CPAP, S) For ST device: 15 L/min (CPAP, S, ST, T) |
| Humidifier performance | Mask Pressure cm H2O (hPa) RH output % at 63°F (17°C) ambient temperature RH output % at 72°F (22°C) ambient temperature Nominal system output AH1 , BTPS2 Setting 4 Setting 8 Setting 4 Setting 8 3 85 100 6 >10 4 85 100 6 >10 10 85 100 6 >10 20 85 90 6 >10 25 85 90 6 >10 |
| NOTE | The manufacturer reserves the right to change these specifications without notice. • The electrical connector end of the heated air tubing is only compatible with the air outlet at the device end and should not be fitted to the mask. • Do not use electrically conductive or antistatic air tubing. • The temperature and relative humidity settings displayed are not measured values. |