A Disposable Latex-Free Nasopharyngeal Airway is a specialized medical device designed to maintain a patent upper airway in conscious, semi-conscious, or sedated patients where oral airway placement is impractical or contraindicated. Crafted from soft, flexible latex-free medical-grade materials (e.g., PVC or TPE), it features a smooth, curved tubular structure with a flanged proximal end and a rounded, atraumatic distal end-engineered to be inserted through the nasal passage into the pharynx, displacing soft tissues and preventing airway obstruction. Its latex-free design eliminates allergy risks, making it a safe and essential tool for healthcare providers in hospitals, ICUs, emergency departments, and pre-hospital care settings.
The device's anatomical curvature aligns with the natural path of the nasal cavity and pharynx, ensuring gentle insertion with minimal discomfort or trauma to nasal mucosa. The soft, flexible material adapts to individual anatomical variations, reducing the risk of nasal irritation or epistaxis (nosebleeds). The flanged proximal end prevents overinsertion and accidental dislodgement, while the hollow lumen maintains unobstructed airflow for spontaneous breathing or supplemental oxygen delivery. Available in a range of sizes to accommodate infants, pediatric patients, and adults, the device is color-coded for rapid size identification-streamlining decision-making in time-sensitive emergencies. It requires no complex assembly: select the appropriate size, lubricate the distal end, insert gently through the nasal passage, and confirm airway patency. Each unit undergoes rigorous quality testing, including dimensional accuracy checks, biocompatibility evaluations, and flexibility verification, complying with ISO 13485, CE, and NMPA standards for safe and reliable airway management.
Product Specification
|
Item |
Description |
|
Application |
Maintains patent upper airway in conscious/semi-conscious/sedated patients; alternative to oral airways for nasal insertion |
|
Type |
Disposable latex-free nasopharyngeal airway |
|
Material |
Medical-grade PVC/TPE |
|
Core Design |
Curved hollow tube, flanged proximal end, rounded atraumatic distal end |
|
Size Range |
Infant (2.5Fr, 3.0Fr, 3.5Fr), Pediatric (4.0Fr, 4.5Fr, 5.0Fr), Adult (5.5Fr, 6.0Fr, 6.5Fr, 7.0Fr, 7.5Fr, 8.0Fr) |
|
Size Identification |
Color-coded hubs (e.g., 6.0Fr: green, 7.0Fr: orange) for quick selection |
|
Length (Distal to Flange) |
Infant (2.5Fr): 50mm; Pediatric (4.0Fr): 70mm; Adult (6.0Fr): 100mm; Adult (8.0Fr): 120mm (varies by size) |
|
Inner Diameter |
2.5Fr: 0.8mm; 4.0Fr: 1.3mm; 6.0Fr: 2.0mm; 8.0Fr: 2.7mm (Fr = French size, 1Fr = 0.33mm) |
|
Sterility |
EO-sterilized |
|
Shelf Life |
3 years |

Product Properties
- Latex-Free Safety: Eliminates latex allergy risks, suitable for patients and healthcare providers with latex sensitivities.
- Anatomical Curvature: Curved design aligns with nasal-pharyngeal anatomy, enabling gentle, atraumatic insertion.
- Soft & Flexible Material: Adapts to individual nasal structures, reducing irritation and epistaxis risk.
- Secure Placement: Flanged proximal end prevents overinsertion and dislodgement during patient care or movement.
- Rapid Size Identification: Color-coded hubs enable quick size selection in emergency scenarios, saving critical time.
- Disposable Convenience: Single-patient use eliminates cross-infection risks; no cleaning or reprocessing required.
- Multi-Scenario Compatibility: Suitable for conscious patients (tolerated better than oral airways) and those with oral trauma or trismus (jaw stiffness).
Application
- Emergency Care: Stabilizes airways in patients with altered mental status, trauma, or overdose where oral airway placement is not feasible.
- ICU & Critical Care: Supports airway management for sedated, ventilated, or critically ill patients (e.g., those with facial burns, oral surgery, or trismus).
- Anesthesia: Used during general anesthesia for patients requiring airway support without oral device interference (e.g., dental procedures).
- Pre-Hospital Care: Essential for ambulance crews and first responders to manage airways in patients with oral trauma or difficulty tolerating oral airways.
- Pediatric & Neonatal Care: Size-adapted, soft-design options for infants and children with delicate nasal and pharyngeal tissues.
- Post-Operative Care: Provides airway support for patients recovering from head, neck, or oral surgeries where oral breathing is compromised.

Physical Properties
|
Item |
Specification |
|
Operating Temperature |
5℃~40℃ |
|
Material Hardness |
Shore A 70-75 |
|
Product Weight |
Size 0: 2.5g; Size 3: 6g; Size 7: 12g |
|
Wall Thickness |
1.2-1.6mm |
|
Transparency |
≥85% light transmittance |
|
Pressure Resistance |
≥35 kPa |
QA&QC

Certifications: Complies with ISO 13485, CE, and NMPA medical device standards. Each production batch undergoes dimensional accuracy testing to ensure consistency across sizes, latex-free verification to confirm no latex contaminants, biocompatibility assessments (cytotoxicity, sensitization) for nasal contact materials, flexibility testing to validate atraumatic insertion, and sterility validation for EO-sterilized units. Unique batch number is assigned for full production and distribution traceability, and detailed Instruction for Use (IFU) is provided.
Packing, Storage, Handling and Transportation
- Packing: Individual EO-sterilized paper-plastic composite packaging (single unit per pack); bulk transport in sturdy corrugated cartons with anti-crush dividers. Each package is labeled with size, French (Fr) number, color code, and sterilization indicator for easy identification.
- Storage: Store in a clean, dry, well-ventilated environment (temperature 5℃~40℃, relative humidity ≤80%). Avoid direct sunlight, high heat, or contact with sharp objects and corrosive substances. Keep packaging intact until immediate use.
- Handling: For single-patient use only-do not reuse, reprocess, or share to prevent cross-infection. Select the correct size based on patient age, weight, or nasal passage diameter; inspect the device for cracks, deformities, or contamination before insertion. Lubricate the distal end with a water-soluble lubricant prior to insertion to minimize tissue irritation.
- Transportation: Transport in accordance with medical device regulations. Protect from violent collision, rain, or moisture to preserve product sterility, structural integrity, and flexibility.
Reasons for choosing us
Zhejiang Mediunion Healthcare Group Co. Ltd. (a branch of Evergrand Healthcare Group, founded in 2014) is located in Ningbo City, Zhejiang Province - enjoying an excellent location and convenient transportation. Our business covers medical device manufacturing & sales, plus investments in nursing homes, dental clinics, specialist hospitals and medical care services. Our products are sold worldwide, and we've won global consumer recognition with high-quality goods and comprehensive after-sales service.

Diversified Product Portfolio
Our product range includes disposable medical consumables, medical equipment and non-woven products (e.g. dental supplies, respiratory care items). This diverse lineup caters to the needs of medical institutions, clinics and other clients.

Reliable Supply & Collaboration
We have rich industry experience and partner with over 600 factories. These partners are equipped with advanced production equipment and skilled frontline staff, enabling us to produce customized products/components as per specific requests.

Strict Quality Assurance
We prioritize innovation & quality, backed by the ISO 13485:2016 quality management system. Strict control runs through raw material procurement, mass production, process management and finished product release. Our professional services (production control, order follow-up, delivery) also set us apart.
Certificate

FAQ
Q:What is your standard production lead time?
A:Our standard production lead time for bulk orders is 3-4 weeks after order confirmation and receipt of the deposit. For large-volume orders (exceeding 100,000 units) or customized products, the lead time may be extended to 4-7 weeks. We will provide a detailed production schedule upon order placement and keep you updated on the production progress in real-time.
Q:Do you have experience shipping to our country/region?
A:Yes, we have extensive experience shipping to countries and regions worldwide, including North America, Europe, Asia, South America, and Africa. We are familiar with the local import regulations, customs clearance requirements, and logistics channels of different regions, and can cooperate with reputable logistics partners (e.g., DHL, FedEx, UPS, or sea freight forwarders) to ensure smooth delivery. We also provide all necessary shipping documents (e.g., commercial invoice, packing list, certificate of origin, and customs clearance documents) to facilitate customs clearance.
Q:How do you ensure proper packaging, labeling, and transport safety?
A:We take multiple measures to ensure packaging, labeling, and transport safety:
Packaging: Use shockproof, moisture-proof, and sterile packaging (if applicable) that meets international shipping standards. For fragile products, we add extra protective materials (e.g., bubble wrap, foam) to prevent damage during transportation;
Labeling: All labels comply with UDI/GS1 and local regulatory requirements, including product name, batch number, expiration date, usage instructions, and warning information. Multilingual labels are available upon request;
Transport Safety: Cooperate with logistics partners with experience in medical product transportation, ensuring compliance with temperature control requirements (if applicable) and providing transport insurance to cover any potential losses during shipment.
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