• Non-adherent, atraumatic dressing changes
• Manages exudate through the dressing while promoting moist wound environment
• Can remain in place for five to seven days
• Easy fixation, good staple retention
• Soft and conforming
• Compatible with topical wound treatments
• May be used with biological/biosynthetic primary dressings
• Suitable for use with NPWT

Rylon-1® is indicated for the management of a wide range of wounds, including superficial or partial-thickness, such as first- and second-degree burns, skin grafts, donor sites, post-operative wounds, skin tears, lacerations, stage 1-4 pressure ulcers, as well as venous, arterial and neuropathic ulcers. Rylon-1® is also suitable as a primary layer to be used in conjunction with other dressing materials.

Rylon-1® is contraindicated for wounds with clinical signs of infection. Inspect wounds daily for infection. If infection occurs, thoroughly cleanse the wound and apply a new dressing. Rylon-1® is contraindicated for patients with known allergies or sensitivities to silicone. Rylon-1® is not intended to be used principally with wounds that have breached the dermis and can only heal by secondary intent. Rylon-1® is contraindicated for primary coverage of third-degree burns. Rylon-1® may be left in place for several days, as long as exudate passes freely into the secondary dressing. Rylon-1® may typically remain on the wound for up to five days, but caution should be exercised that the wound does not become dry, as this may lead to adherence of the dressing to the wound bed.

This is a single-use product. Reuse of this product would likely cause infection and may lead to serious injury up to and including death.

Store dressings away from direct sunlight at ambient temperature and humidity.
Sterile unless individual package is damaged or opened.