• Soft, conformable, multi-layered dressings containing superabsorbent fibers and Hydrofiber® Technology
• Aquacel® Hydrofiber® Technology responds by gelling on contact with wound exudate to maintain a moist wound environment, vertically wicking to reduce risk of maceration and micro-contouring to minimize dead space where bacteria can proliferate
• ConvaFoam™ Silicone and Border feature an enhanced silicone with improved skin-friendly adhesion
• Superabsorbent fibers increase the fluid handling capacity of the family of dressings
• Outer film layer provides a showerproof barrier to viruses and bacteria that also aids in the management of moisture vapor transmission of exudate absorbed by the dressing

ConvaFoam™ Border, Silicone and Non-Adhesive dressings may be used for the management of exuding and non-exuding wounds and for the protection of intact skin. ConvaFoam™ dressings are indicated for the treatment of wounds such as leg ulcers, pressure ulcers, diabetic foot ulcers, surgical wounds, and traumatic wounds. Additionally, ConvaFoam™ Border and Non-Adhesive may be utilized as part of the treatment of partial-thickness burns. The dressings may be used as a primary or secondary dressing.

ConvaFoam™ dressings should not be used on individuals who are sensitive to or who have had an allergic reaction to the dressing or components of the dressing. ConvaFoam™ dressings are not compatible with oxidizing agents such as hydrogen peroxide or hypochlorite solutions.

ConvaFoam™ Silicone, Border and Non-Adhesive dressings are for single use only. Do not reuse. Reuse may lead to increased risk of infection, cross-contamination and delayed healing. This dressing should not be used with out wound care products without first consulting a health care professional. ConvaFoam™ dressings should not be submerged during bathing or swimming. For highly exuding wounds, ConvaFoam™ Border or Non-Adhesive dressings may be used as a secondary dressing in conjunction with a primary dressing such as Aquacel® silver and non-silver Hydrofiber® products. Consult a health care professional if any of the following are observed:
• Irritation (reddening, inflammation)
• Maceration (whitening of skin)
• Hyper-granulation (excess tissue formation)
• Sensitivity or allergic reaction
• Signs of infection occur (increased pain, bleeding, wound drainage)
• Changes in wound color and/or odor
• Increase in wound size
• Wound not showing signs of healing
After use, this product may be a potential biohazard. Handle and dispose of in accordance with accepted medical practice and applicable local laws and regulations. If during the use of this device or as a result of its use a serious incident has occurred, please report it to the manufacturer.

If further information or guidance is needed, or to report an adverse event, please contact Convatec.

Store at room temperature. Protect from light. Keep dry. Ensure the dressing pouch is not damaged or opened prior to use to guarantee sterility. If the dressing pouch is damaged or open, do not use and dispose according to local regulations. Do not use after expiry date.

Sodium carboxymethylcellulose, polyurethane foam, superabsorbent fibers, polyurethane film, silicone adhesive (Silicone and Border versions)