
Airways Surgicals Airoventuri Venturi Mask
Pack Sizes Available
Product Description
Technical Specifications
- Device Type: High-flow air-entrainment oxygen delivery system (Venturi mask)
- Operating Principle: Venturi effect air-entrainment for precise FiO2 delivery independent of breathing pattern
- Oxygen Concentrations Available: 24%, 28%, 31%, 35%, 40%, 50%, (60% with optional red diluter)
- Color-Coded Diluters: Blue (24%), Yellow (28%), White (31%), Green (35%), Pink (40%), Orange (50%), Red (60%)
- Flow Rate Requirements: 2-4 L/min (24%), 4-6 L/min (28-35%), 8-10 L/min (40-50%), 10-12 L/min (60%)
- Total Flow Delivered: 30-60 L/min (oxygen plus entrained air), meets patient inspiratory demand
- Mask Material: Medical-grade transparent PVC, soft anatomical molding
- Tubing: 7 feet (2.1 meters) crush-resistant star lumen oxygen supply tubing with universal connector
- Available Sizes: Adult (standard), Pediatric (available separately)
- Mask Features: Adjustable nose clip, elastic headstrap, elongated chin design, soft cushioned edges
- Latex Content: Latex-free for enhanced patient safety
- Clinical Applications: COPD exacerbations, controlled oxygen therapy, post-operative recovery, pneumonia, hypoxemia requiring precision FiO2
- Package Contents: 1 mask, 6-7 color-coded diluters, 7 ft oxygen tubing, elastic headstrap, instructions
- Sterilization: Non-sterile (oxygen therapy device, not surgical), individually packaged
- Usage: Single-use, single-patient disposable only
- Regulatory: Medical device meeting ISO standards for oxygen therapy equipment
Frequently asked questions
A Venturi mask is a high-flow oxygen delivery system that provides precise, controlled oxygen concentrations (FiO2) from 24% to 60%. It works using the Venturi principle: high-velocity oxygen flows through a narrow jet, creating negative pressure that entrains room air at a fixed ratio. Different color-coded diluters have specific port geometries that control the air-to-oxygen mixing ratio. This engineering ensures consistent FiO2 delivery regardless of variations in patient breathing patterns, tidal volumes, or inspiratory flow demands, unlike simple masks or nasal cannulas where oxygen concentration varies with breathing.
Each color-coded diluter delivers a specific oxygen concentration at a designated flow rate: Blue = 24% O2 at 2-4 L/min, Yellow = 28% O2 at 4-6 L/min, White = 31% O2 at 4-6 L/min, Green = 35% O2 at 4-6 L/min, Pink = 40% O2 at 8-10 L/min, Orange = 50% O2 at 8-10 L/min, and Red (when included) = 60% O2 at 10-12 L/min. The color coding system prevents selection errors during emergencies and ensures clinicians can quickly identify and attach the correct diluter for prescribed oxygen therapy without consulting reference charts.
Venturi masks are preferred for COPD patients because they prevent over-oxygenation, which can suppress the hypoxic respiratory drive that many chronic COPD patients depend on for breathing stimulus. COPD patients with chronic CO2 retention can become dependent on low oxygen levels (hypoxemia) to trigger breathing. If given too much oxygen with imprecise delivery devices, their respiratory drive can decrease dangerously. Venturi masks allow precise titration starting at 24-28% oxygen with gradual increases as clinically indicated, avoiding the risk of sudden respiratory depression from uncontrolled high oxygen delivery.
High-flow oxygen devices like Venturi masks provide total gas flow (oxygen plus entrained air) that meets or exceeds peak inspiratory flow demand, typically 30-60 L/min depending on diluter. This means the patient breathes only the gas mixture from the device, ensuring precise FiO2. Low-flow devices like nasal cannulas or simple masks deliver oxygen at 1-15 L/min, which is less than inspiratory demand (30-40 L/min during distress). The patient dilutes the oxygen by inhaling additional room air (21% O2), making actual FiO2 unpredictable and variable with breathing patterns.
Venturi masks are designed and intended as single-use, single-patient disposable devices. They must NOT be reused or resterilized. Each patient must receive a new sterile mask. Reusing these devices introduces unacceptable infection control risks including healthcare-associated pneumonia, cross-contamination between patients, biofilm accumulation on mask surfaces and in tubing that cannot be adequately cleaned, and material degradation that may affect oxygen delivery accuracy or structural integrity. Proper disposal as biohazard waste after single use is mandatory.
To assemble: (1) Select the appropriate color-coded diluter for the prescribed oxygen concentration, (2) Attach the diluter firmly to the mask body, ensuring it locks in place, (3) Connect the oxygen supply tubing to the diluter port, (4) Set the oxygen flowmeter to the flow rate indicated on the diluter (e.g., 4-6 L/min for 28%), (5) Place the mask over the patient's nose and mouth with the elongated portion under the chin, (6) Adjust the nose clip for comfortable seal, (7) Secure with elastic headstrap behind the head. Verify oxygen is flowing and patient is breathing comfortably. Monitor for proper seal and adequate oxygenation.
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 Airopop CPAP Nasal Mask
Sleep apnea therapy fails for most patients not because the machine delivers inadequate pressure. Not because the prescription was wrong. It fails because the mask is uncomfortable enough that patients find reasons not to wear it every night. Pressure points on the nasal bridge by 2 AM. Strap marks still visible at breakfast. Air leaks every time you shift position. These are the small frustrations that accumulate until the expensive CPAP machine gathering dust in the closet becomes just another abandoned medical device that technically works but nobody actually uses. Airways Surgicals Airopop nasal mask was designed to address the comfort barriers that undermine CPAP therapy compliance. This is a lightweight nasal interface mask designed for continuous positive airway pressure (CPAP) therapy in patients diagnosed with obstructive sleep apnea (OSA). The mask covers only the nose, delivering pressurized air through soft silicone cushions that create a seal around the nasal area while leaving the mouth free and unobstructed. This minimalist design is preferred by nasal breathers who find full-face masks claustrophobic and prefer less facial coverage during sleep. The soft silicone nasal cushion features a dual-wall construction that conforms to individual facial contours without requiring excessive strap tension. This cushion technology distributes seal pressure evenly across the contact surface rather than concentrating force on pressure points like the nasal bridge, which is the primary complaint causing mask abandonment. The cushion is available in multiple sizes (Small, Medium, Large) because proper sizing is critical for both comfort and seal effectiveness. An incorrectly sized cushion either leaks or requires overtightening to maintain seal. The adjustable four-point headgear system uses soft elastic straps with Velcro adjustment that allows independent tuning of upper and lower strap tension. This granular adjustability accommodates different head shapes and sizes while maintaining stable mask position throughout the night despite sleep position changes. The quick-release clips allow mask removal without readjusting straps, which is valuable for middle-of-night bathroom breaks or when briefly removing the mask is necessary. The lightweight frame minimizes the sensation of wearing equipment on your face. Heavier masks create fatigue and pressure awareness that interferes with sleep initiation. The rigid frame component maintains cushion shape and position while the minimal design reduces overall weight to barely noticeable levels once patients acclimate. The swivel elbow connection at the frame allows tubing rotation without torquing the mask seal. This feature accommodates different sleeping positions and tubing routing preferences without generating the twisting forces that break seal integrity and cause leaks. Active sleepers who change position frequently benefit considerably from this rotational freedom. The exhalation port features diffuser technology that disperses exhaled air quietly to minimize disturbance to bed partners. Early CPAP masks were notoriously loud, creating enough air turbulence noise to wake anyone sleeping nearby. Modern diffuser design redirects exhaled air in a pattern that reduces noise while maintaining proper CO2 washout. For distributors supplying sleep medicine clinics, home medical equipment providers, and respiratory therapy departments, nasal CPAP masks represent essential durable medical equipment with replacement cycles driven by cushion wear. Sara Wellness has been exporting sleep apnea therapy equipment and respiratory care devices 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.