Description

The PHILIPS NEOPLEX BOUGIE is a versatile medical device designed for specialized clinical settings. It serves multiple critical functions, primarily in the fields of urethral management and airway management. This device is essential for healthcare professionals dealing with complex medical scenarios, such as urethral stricture management and challenging tracheal intubations.

Key Features

• Urethral Management: The bougie is adept at non-endoscopic urethral expansion and dilation, making it invaluable for traversing and exploring urethral strictures. Its design includes features like a straight or tapered olive tip, which can be bent or contoured to navigate through strictures effectively.

• Airway Management: As an endotracheal tube introducer, it assists in tracheal intubation, especially in difficult airway situations or during CPR. It is suitable for use with direct or video laryngoscopy, supraglottic airway devices, and other advanced airway techniques.

Design Specifications

• Material Composition: Typically constructed from Neoplex material or PVC, with some models featuring a threaded metal section. This robust construction ensures durability and reliability.

• Size Variability: Available in various Charriere sizes and lengths, including typical introducer sizes of 10 or 15 French, with lengths ranging from 600 to 700 mm. Some versions include a 'hockey-stick' coude tip and external distance markings for enhanced functionality.

• Connectability: Certain models are threaded at the proximal end to connect with a filiform follower, enhancing their versatility in clinical applications.

Packaging and Sterilization

Each bougie is individually packaged and sterile, ensuring readiness for immediate use. Most models are packaged individually, while some are available in boxes of 5 or 10 units, maintaining high standards of hygiene and convenience.

Precautions

Healthcare professionals should be aware of potential complications such as airway trauma or device fracture. Proper handling and adherence to clinical guidelines are essential to mitigate risks. The device is not intended for use as a trocar and should not be used to puncture the pleura.

Regulatory Information

The PHILIPS NEOPLEX BOUGIE is classified under EMDN code L06050101 and GMDN code 11704, aligning with international medical device standards. This classification underscores its specialized role in healthcare settings, providing assurance of its quality and compliance.

This device is non-returnable, emphasizing the importance of precise selection and usage within its intended clinical scope. The PHILIPS NEOPLEX BOUGIE stands as a critical tool for medical professionals, offering precision and reliability in demanding healthcare environments.