• Clean one piece removal
• Effective fluid management
• Comfortable gel matrix with minimal shrinkage
• Minimal nursing time for dressing changes
• Up to 7 day wear time
• Sustained antimicrobial activity (in vitro)
• May help reduce associated costs of infection

DURAFIBER* Ag Silver Gelling Fiber Dressings are indicated for chronic and acute, partial- or full-thickness or shallow granulating exuding wounds including: leg ulcers, pressure injuries, diabetic ulcers, surgical wounds, wounds left to heal by secondary intent, donor sites, tunneling and fistula wounds, partial-thickness burns, traumatic wounds, and wounds that are prone to bleeding, such as wounds that have been surgically or mechanically debrided.

Do not use on patients with a known sensitivity to silver. Do not use on non-exuding wounds.

While DURAFIBER* Ag assists in the management of wounds prone to bleeding, it is not intended to be used as a surgical sponge in heavily bleeding wounds. If reddening or sensitization occurs discontinue use. DURAFIBER* Ag is not compatible with oil-based products such as petrolatum. Avoid contact with electrodes or conductive gels during electronic measurements (eg, EEG and ECG). Ensure that packing in cavities, sinuses, etc has been removed. The dressing may not be compatible with topical antimicrobials. In the event of clinical infection, topical silver does not replace the need for systemic therapy or other adequate infection treatment. When DURAFIBER* Ag is used on a patient during MRI (Magnetic Resonance Imaging) examination, some warming may be experienced. DURAFIBER* Ag may cause transient discoloration of the surrounding skin.