Description

The AIRTRAQ SP is an innovative, single-use video laryngoscope designed by Airtraq to enhance tracheal intubation procedures. Its anatomically shaped, channeled blade provides healthcare professionals with a clear view of the airway, facilitating accurate endotracheal tube placement even in challenging scenarios. This device is particularly beneficial for patients with limited neck mobility or those requiring intubation in non-standard positions.

Key Features

• Disposable Design: The single-use nature of AIRTRAQ SP reduces the risk of cross-contamination and eliminates the need for device cleaning.
• Enhanced Visualization: Offers multiple viewing options, including compatibility with eyecups, WiFi cameras, and smartphone adapters, providing a magnified view of the larynx.
• Built-in Anti-fog System: Automatically activates with LED illumination to ensure a clear view during intubation.
• Portability: Lightweight and ready to use straight from the package, making it ideal for emergency situations and use in remote locations.

MRI Compatibility

The device is MR conditional, safe for use in MRI environments up to a 3-Tesla static magnetic field, though not intended for use inside the scanner bore during operation.

Power and Battery Life

Powered by non-replaceable AAA batteries, AIRTRAQ SP offers a minimum of 40 minutes of continuous use, with a blinking indicator to signal battery depletion. The device has a shelf life of up to three years from packaging.

Intubation Technique

The AIRTRAQ SP allows for intubation with the patient's head in a neutral position, guiding the endotracheal tube through a lateral channel towards the glottis. It is compatible with standard endotracheal tubes, requiring minimal adjustment for clinicians.

Storage and Disposal

Store the device between -5°C and 55°C with relative humidity levels of 10–95%. After use, dispose of the device as potentially contaminated waste, ensuring the battery is not incinerated with the device.

Regulatory Information

The AIRTRAQ SP holds FDA 510(k) clearance and complies with relevant medical device standards, ensuring it meets safety and performance requirements. It is intended for use by trained healthcare professionals, with clear instructions to avoid misuse.

This comprehensive tool is designed to improve airway management outcomes, providing reliable performance across a range of clinical settings.