Description

The PHILIPS NEOPLEX BOUGIE, offered by Coloplast, is a specialized medical device crafted for healthcare professionals in advanced clinical settings. This versatile instrument is designed for the non-endoscopic expansion of urethral strictures, making it an essential tool in urological procedures. Its primary functions include traversing and exploring urethral strictures, gradual dilation of these strictures, and dilation of the meatus prior to endoscopy.

Key Features

• Filiform Bougie Design: The device is extremely thin, wire-like, and flexible, allowing it to be bent or contoured to facilitate passage through difficult-to-cross strictures. This flexibility is crucial for effective treatment, resuscitation, palliative care, and surgical applications.

• Variety of Tips: The bougie may feature a bulbous (olive tip), straight, spiral, or coudé tip, enhancing its adaptability to different clinical needs. The proximal end may be threaded to connect to a filiform follower, providing additional functionality.

• Material Composition: Constructed from durable plastic materials such as polyvinyl chloride (PVC) or Neoplex material, complemented by a threaded metal section. This robust construction ensures longevity and reliability.

Variants and Sizes

• Female Metric Thread: Available in lengths of 34 cm with sizes ranging from CH 8 to CH 24.
• Male Metric Thread: Available in lengths of 30 cm with sizes ranging from CH 3 to CH 7.
• Catheters with Female Metric Thread: Length of 40 cm, sizes from CH 8 to CH 24.

The general size range spans Charriere 6 to 30, accommodating a wide array of clinical requirements.

Packaging and Sterility

Each bougie is individually packaged to maintain sterility, with some variants available in boxes of 5 or cartons of 100. The device is reusable, does not require refrigeration, and is classified as a capital item, underscoring its long-term value in medical practice.

Clinical Suitability

The PHILIPS NEOPLEX BOUGIE is suitable for use across all sexes and demands specialized clinical knowledge, ensuring it is employed effectively in the appropriate medical contexts. Its design and material attributes align with the rigorous standards expected in specialized outpatient services and hospital environments.

Classification

The device is classified under EMDN code L06050101 and GMDN code 11704, reflecting its specific application in the medical field. GST applicability is noted, aligning with standard medical device regulations.

This comprehensive tool enhances the capabilities of healthcare providers, offering precision and reliability in the management of urethral strictures.