Smiths Medical 100/783/090 - TUBE TRACHEOSTOMY SIZE 9MM CUFFED FENESTRATED 87MM PVC FLEXIBLE NECK FLANGE DUAL-AXIS SWIVEL ADAPTER OBTURATOR TRACH-TIE DECANNULATION CAP PORTEX RADIOPAQUE STERILE

Smiths Medical 100/783/090 - TUBE TRACHEOSTOMY SIZE 9MM CUFFED FENESTRATED 87MM PVC FLEXIBLE NECK FLANGE DUAL-AXIS SWIVEL ADAPTER OBTURATOR TRACH-TIE DECANNULATION CAP PORTEX RADIOPAQUE STERILE

The Smiths Medical 100/783/090 tracheostomy tube is designed to support secure airway management in patients requiring long-term or intermediate tracheostomy care. Featuring a 9mm internal diameter and fenestrated design, this tube allows for improved airflow and supports speech when clinically appropriate. Constructed from high-quality radiopaque PVC, it provides flexibility and patient comfort while ensuring visibility during imaging procedures. The integrated cuff enhances airway sealing, while the flexible neck flange ensures a comfortable and stable fit for varying patient anatomies. This complete sterile set includes a dual-axis swivel adapter, obturator, trach tie, and decannulation cap for comprehensive airway management.

Key Benefits

The fenestrated design facilitates airflow through the upper airway, supporting phonation and improving patient communication. The cuffed configuration provides an effective seal for controlled ventilation and reduces the risk of aspiration. The flexible neck flange enhances patient comfort and minimizes pressure on the stoma site. The dual-axis swivel adapter allows for greater mobility and reduces tubing strain during patient movement. Radiopaque material ensures clear visibility during X-ray procedures, enhancing clinical monitoring and safety.

Compatibility and Applications

This tracheostomy tube is suitable for use in hospitals, long-term care facilities, and home care environments. It is compatible with standard ventilators, humidification systems, and suction equipment. Commonly used in intensive care units, respiratory therapy, and post-surgical airway management, it supports patients requiring controlled ventilation, airway protection, or weaning from mechanical ventilation.

Usage Guidelines

The device should be inserted by trained healthcare professionals following established tracheostomy procedures. The obturator is used during insertion to facilitate smooth placement and must be removed immediately after positioning. Cuff inflation should be carefully monitored to maintain an adequate seal without excessive pressure. Regular inspection and cleaning of the tube are essential to maintain airway patency and reduce infection risk. The fenestration should be used only when clinically appropriate and under professional supervision.

Certifications and Safety Standards

This product is manufactured in compliance with recognized international medical device standards. It is supplied sterile and is intended for single-patient use. The materials used are biocompatible and designed to meet stringent safety and performance requirements in clinical environments.

Comparison with Competitors

Compared to standard non-fenestrated tracheostomy tubes, this model provides enhanced functionality by enabling airflow through the upper airway, supporting speech and improved patient comfort. The inclusion of a dual-axis swivel adapter offers greater flexibility compared to fixed connectors found in many alternative products. The flexible flange design also provides a more adaptive fit, reducing discomfort and improving long-term usability.

Typical User Profile and Application Scenarios

This product is ideal for patients requiring prolonged airway access, including those recovering from respiratory failure, neurological conditions, or head and neck surgeries. It is frequently used in intensive care settings, step-down units, and home care environments where ongoing airway management and patient comfort are essential.

Best Practices for Use and Maintenance

Routine monitoring of cuff pressure is recommended to prevent tissue damage and ensure effective ventilation. The tracheostomy site should be regularly assessed for signs of infection or irritation. The tube and accessories should be cleaned or replaced according to clinical protocols. Proper securing of the tube using the provided trach tie helps prevent accidental displacement.

Regulatory and Safety Information

This device is intended for use by qualified healthcare professionals trained in airway management. It should be used in accordance with institutional protocols and manufacturer guidelines. Any signs of damage, contamination, or malfunction should be addressed immediately by replacing the device.

How to Order

Select the Smiths Medical 100/783/090 TUBE TRACHEOSTOMY SIZE 9MM CUFFED FENESTRATED 87MM PVC FLEXIBLE NECK FLANGE DUAL-AXIS SWIVEL ADAPTER OBTURATOR TRACH-TIE DECANNULATION CAP PORTEX RADIOPAQUE STERILE, and add it to your cart. Complete checkout with your preferred shipping and payment options. For bulk orders, quotes, or further assistance, contact CIA Medical customer service at (312)275-5850 or use the contact form on this page.