
Airways Surgicals Airopop CPAP Nasal Mask
Pack Sizes Available
Product Description
Technical Specifications
- Mask Type: Nasal interface CPAP mask for obstructive sleep apnea therapy
- Coverage Area: Nose only (does not cover mouth)
- Cushion Material: Medical-grade soft silicone with dual-wall construction
- Available Cushion Sizes: Small, Medium, Large (proper sizing critical for seal and comfort)
- Frame Material: Lightweight rigid polycarbonate or medical-grade plastic
- Headgear Configuration: Four-point adjustable elastic headgear with Velcro adjustment
- Headgear Features: Quick-release clips for removal without readjusting straps
- Elbow Connection: 360-degree swivel elbow for tubing rotation without seal torque
- Exhalation Port: Integrated diffuser technology for quiet exhalation
- Tubing Compatibility: Standard 22mm CPAP tubing connection (universal fit)
- Weight: Lightweight design for minimal facial awareness during sleep
- Pressure Range: Suitable for 4-20 cmH2O (standard CPAP pressure range)
- Ideal For: Nasal breathers, side sleepers, back sleepers, patients preferring minimal facial coverage
- Not Recommended For: Mouth breathers, patients with chronic nasal congestion, severe allergies
- Replacement Schedule: Cushion: 1-3 months, Headgear: 6 months, Frame: 6-12 months
- Cleaning: Daily wipe, weekly wash with mild soap and water, air dry
- Regulatory: Medical device for sleep apnea therapy, may require prescription depending on region
Frequently asked questions
A CPAP nasal mask is an interface device that covers only the nose and delivers continuous positive airway pressure for treating obstructive sleep apnea (OSA). It's ideal for patients who primarily breathe through their nose during sleep, prefer less facial coverage than full-face masks, do not have chronic nasal congestion or allergies, and find nasal pillows uncomfortable at higher pressure settings. Nasal masks provide a good middle ground between minimal nasal pillow interfaces and more bulky full-face masks, offering effective therapy with moderate facial contact.
Proper cushion sizing is critical for both comfort and effective seal. Most manufacturers provide sizing gauges or guides to measure your nose dimensions. Generally: Small fits petite facial features and smaller noses, Medium fits average adult facial dimensions (most common size), and Large fits broader facial features and larger noses. The cushion should create a seal without excessive strap tension—if you need to overtighten straps to prevent leaks, try the next size down. If the cushion feels too tight or leaves deep marks, try the next size up. Many suppliers offer fit kits with multiple sizes to try before committing.
Common causes of mask leaks include: incorrect cushion size (too large or too small), overtightened or undertightened headgear straps, cushion wear or damage (silicone degrades over time and should be replaced every 3-6 months), facial hair interfering with seal, sleeping position putting pressure on mask frame, weight changes affecting facial dimensions, and dirty cushions where skin oils reduce seal effectiveness. Troubleshooting involves checking cushion condition, adjusting strap tension evenly, ensuring proper size, and maintaining a clean cushion. Persistent leaks despite troubleshooting may indicate need for cushion replacement or different mask style.
Recommended replacement schedule: Nasal cushions every 1-3 months (or when they lose elasticity, become stiff, or develop visible wear), Headgear every 6 months (or when straps lose elasticity and no longer hold mask securely), Complete mask frame every 6-12 months (or if damaged/cracked). More frequent replacement may be needed for users with oily skin, those who sweat heavily during sleep, or if components are not cleaned regularly. Insurance typically covers these replacements on similar schedules. Regular replacement maintains optimal seal, comfort, and therapy effectiveness.
Nasal CPAP masks are designed for nose breathers. If you breathe through your mouth during sleep, pressurized air will escape through your open mouth, causing: therapy ineffectiveness (pressure doesn't reach your airway), severe dry mouth, inability to maintain prescribed pressure, and excessive air leakage triggering machine alarms. Mouth breathers should use full-face masks that cover both nose and mouth. If you prefer nasal masks, you can try using a chinstrap to keep your mouth closed, though this doesn't work for everyone. Consult your sleep specialist before switching mask types.
Daily cleaning: Each morning, wipe the cushion with unscented baby wipes or a damp cloth to remove facial oils. Weekly cleaning: Disassemble mask (remove cushion and headgear from frame), hand wash all components in warm water with mild, fragrance-free soap (dish soap works well), rinse thoroughly to remove all soap residue, air dry on a clean towel out of direct sunlight. Never use harsh chemicals, bleach, alcohol, or put mask components in the dishwasher or washing machine. Replace components if they develop an odor, discoloration, stiffness, or visible wear despite cleaning. Proper maintenance extends component life and ensures effective therapy.
Related Products
Explore more high-quality items from our Respiratory and Anaesthesia range.

Airways Surgicals Airomount Catheter Mount
Ventilated patients require a connection between their endotracheal tube and the breathing circuit that does more than simply join two pieces of equipment. That connection must absorb the weight of heavy circuit tubing so it doesn't drag on the ET tube and traumatize the trachea. It needs to provide flexibility for patient repositioning without disconnecting the airway. It should allow suctioning and bronchoscopy access without breaking the circuit seal. Standard rigid connectors fail at all three requirements, which is why tracheal injuries from tube displacement remain a persistent ICU complication. Airways Surgicals Airomount catheter mounts were engineered specifically to solve these mechanical stress points in ventilated patient management. This is a flexible tubular connector designed to link the patient's endotracheal tube or tracheostomy tube to the breathing circuit in anesthesia delivery systems, mechanical ventilators, and resuscitation equipment. The primary function is transferring the weight and drag of the breathing circuit away from the airway device, minimizing traction and torque forces on the ET tube that can cause tracheal mucosal injury, tube migration, or accidental extubation during patient care activities. The double swivel elbow configuration provides rotational freedom at both ends of the mount. This dual-articulation design allows the breathing circuit to be positioned optimally without transmitting rotational forces to the ET tube. Clinical staff can reposition patients, adjust circuit angles, or accommodate surgical field requirements without fighting against rigid connections that want to twist the airway back to their preferred geometry. The collapsible corrugated tubing construction (in corrugated models) provides axial flexibility while maintaining structural integrity under positive and negative pressure. The corrugations allow the tube to extend, compress, and bend without kinking or collapsing, which is critical during patient transport, surgical positioning changes, or when accommodating different patient sizes and bed heights. Smooth bore variants offer lower airflow resistance for patients requiring minimal dead space. The suction port with flip-top cap (when present) enables closed-system suctioning without disconnecting the breathing circuit. This maintains PEEP (positive end-expiratory pressure) during suctioning procedures, prevents alveolar de-recruitment that occurs with open suctioning, and reduces staff exposure to aerosolized pathogens. The tethered cap design ensures the port remains clean when not in use and cannot be misplaced. Standard 15mm ID / 22mm OD connectors ensure universal compatibility. The patient end features a 15mm female connector that fits all standard endotracheal and tracheostomy tubes. The circuit end features a 22mm female / 15mm male connector compatible with all breathing system Y-pieces, HME filters, and ventilator circuits meeting ISO standards. The transparent material allows visual confirmation of condensate accumulation and secretions within the mount, alerting staff when replacement is needed to maintain optimal airflow and prevent infection risks from contaminated equipment. Individual sterile packaging ensures infection control compliance for single-patient use, which is now standard practice in most facilities to prevent ventilator-associated pneumonia and cross-contamination. For distributors supplying intensive care units, operating rooms, anesthesia departments, and respiratory therapy services, catheter mounts represent essential respiratory consumables with predictable usage tied to ventilated patient census. Sara Wellness has been exporting respiratory and anesthesia supplies from India for 15 years.

Airways Surgicals Airoventuri Venturi Mask
Oxygen therapy for COPD patients operates under a paradox that standard oxygen delivery systems cannot accommodate. Give too much oxygen and you risk suppressing the hypoxic respiratory drive that keeps these patients breathing. Give too little and hypoxemia worsens. Simple masks and nasal cannulas offer no precision here, just rough approximations that force clinicians to titrate blindly and hope physiological monitoring catches problems before they become crises. The margin between therapeutic and harmful oxygen concentration can be as narrow as five percentage points. Venturi masks solve this control problem through engineering that standard oxygen delivery devices ignore entirely. This is a high-flow oxygen delivery system designed to provide precise, controlled oxygen concentrations (FiO2) ranging from 24% to 60% regardless of patient breathing pattern variations. The mask uses air-entrainment technology based on the Venturi principle, where high-velocity oxygen flow through a narrow jet creates negative pressure that entrains room air at a fixed ratio, diluting pure oxygen to predetermined concentrations. This principle-based dilution ensures consistent FiO2 delivery even when tidal volumes, respiratory rates, or inspiratory flow demands fluctuate. The color-coded diluters are where precision lives in this system. Each diluter is engineered with specific port geometry that determines the air-to-oxygen mixing ratio. Blue delivers 24% oxygen at 2-4 L/min flow. Yellow delivers 28% at 4-6 L/min. White delivers 31%. Green delivers 35%. Pink delivers 40% at 8-10 L/min. Orange delivers 50%, and some kits include red for 60% at 10-12 L/min. The color coding prevents selection errors during emergency situations where grabbing the correct diluter must happen instantly without consulting reference charts. The high-flow characteristic matters clinically because total flow (oxygen plus entrained air) meets or exceeds patient inspiratory flow demand. Low-flow devices like nasal cannulas deliver oxygen at 1-6 L/min, but patients can inhale at 30-40 L/min during respiratory distress. The gap gets filled by room air (21% oxygen) diluting whatever the cannula delivers. Venturi systems provide total flows of 30-60 L/min depending on diluter selection, eliminating room air dilution and maintaining precise FiO2. The transparent PVC mask construction allows visual monitoring of facial color, lip position, and secretions without removing the mask. The soft, anatomically-molded design with cushioned edges minimizes pressure points during extended use. The adjustable nose clip and elastic headstrap provide secure positioning without excessive tightness. The elongated style extends under the chin, improving seal without claustrophobic full-face coverage. The 7-foot oxygen supply tubing is crush-resistant with star lumen design that maintains patency even when kinked or compressed. This length provides mobility for patient repositioning without disconnecting oxygen supply. Barbed fittings at connections prevent accidental disconnection during use. Venturi masks are preferred in COPD exacerbations, post-operative recovery requiring controlled oxygenation, pneumonia with hypoxemia risk, and any condition where oxygen toxicity or CO2 retention are clinical concerns. The device is latex-free, single-use disposable, and individually packaged. For distributors supplying respiratory therapy departments, emergency rooms, intensive care units, and home oxygen providers, Venturi masks represent essential controlled oxygen delivery devices. Sara Wellness has been exporting respiratory therapy equipment and oxygen delivery systems from India for 15 years.

Airways Surgicals Resuscitator Ambu Bag (BVM Manual Resuscitator)
Emergency ventilation during cardiac arrest or respiratory failure comes down to a manual skill that nobody practices enough until the moment they desperately need it. Squeeze too hard and you rupture alveoli or fill the stomach with air, triggering aspiration. Squeeze too gently and the patient gets inadequate tidal volumes while cerebral hypoxia accumulates by the second. Maintain improper head position and the airway occludes despite perfect bag technique. These are failures that happen in real emergencies when trained providers discover that occasional simulation training does not translate to confident performance under actual code blue pressure. Airways Surgicals resuscitator bags exist because patients in respiratory arrest need immediate positive pressure ventilation regardless of whether trained providers feel confident delivering it. This is a self-inflating manual resuscitator (bag-valve-mask or BVM) designed to provide emergency positive pressure ventilation to patients with absent or inadequate spontaneous breathing during cardiac arrest, respiratory failure, anesthesia induction, and pre-hospital emergency care. The device consists of a self-inflating bag (available in adult 1600ml, pediatric 550ml, or infant 280ml capacities), a non-rebreathing patient valve, a transparent face mask with cushioned seal, and an oxygen reservoir bag that allows delivery of near-100% oxygen when connected to a supplemental oxygen source. The self-inflating bag features an internal spring mechanism that automatically re-expands after manual compression, drawing in ambient air or oxygen from the reservoir for the next breath. This self-inflation characteristic distinguishes these devices from anesthesia bags that require continuous gas flow to remain inflated. The bag can function entirely without electricity or external gas supply, making it suitable for field use where no infrastructure exists. The non-rebreathing valve directs fresh gas flow to the patient during inspiration while venting exhaled CO2 to atmosphere during expiration, preventing rebreathing. The valve design is critical to device performance. Some models use single shutter valves that close the expiratory port during spontaneous inspiration, preventing room air entrainment. Others use duckbill valves with separate expiratory discs. The specific valve design affects oxygen delivery performance, particularly in spontaneously breathing patients. The transparent anatomically-molded face mask with air-cushioned seal provides the interface between device and patient. The cushion compresses to conform to facial contours, creating a seal without excessive pressure. Mask sizing is critical: adult masks fit patients over 88 lbs, pediatric masks fit children 10-50 kg, infant masks fit neonates and small infants. The transparent construction allows visual confirmation of lip color, secretions, and vomit. The oxygen reservoir bag (typically 2600ml for adult systems) attaches to the gas inlet and fills with oxygen when connected to a flow source at 10-15 L/min. With reservoir attached and high oxygen flow, the device can deliver FiO2 approaching 90-100%. Without reservoir, the device delivers approximately 40-50% oxygen even with supplemental flow, as ambient air mixes with oxygen during bag self-inflation. Optional PEEP (positive end-expiratory pressure) valves attach to the exhalation port to maintain positive airway pressure during expiration, which can improve oxygenation in specific clinical situations during resuscitation. These devices are used in crash carts, ambulances, emergency departments, operating rooms, ICUs, and any location where emergency airway management capability is required. Both reusable (autoclavable) and single-use disposable versions exist. For distributors supplying emergency medical services, hospitals, clinics, and first responder organizations, manual resuscitators represent critical life-saving equipment with predictable replacement cycles. Sara Wellness has been exporting emergency resuscitation equipment and respiratory devices from India for 15 years.