DuoDERM® CGF® Dressing

• Promotes granulation and facilitates autolytic debridement
• Can be easily and gently molded into place
• Can be worn for up to seven days

DuoDERM® CGF® Dressing may be used for minor abrasions, lacerations, minor cuts, minor scalds and burns, and skin tears.
Under the supervision of a health care professional, DuoDERM® CGF® Dressing may be used for wounds such as: leg ulcers (venous stasis ulcers, arterial ulcers and leg ulcers of mixed etiology), diabetic ulcers and pressure ulcers (partial- and full-thickness); surgical wounds (post-operative, donor sites, dermatological excisions); burns (first- and second-degree); traumatic wounds. Minimizes the potential of exposure to nosocomial or infectious agents.

Should not be used on individuals who are sensitive to or who have had an allergic reaction to the dressing or its components.

Caution: Sterility is guaranteed unless package is damaged or opened prior to use. Single use only.
Do not use this product in combination with other wound care products without first consulting a health care professional.
During the body's normal healing process, unnecessary material is removed from the wound, which could make the wound appear larger after the first few dressing changes. If the wound continues to get larger after the first few dressing changes, consult a health care professional.
Should you observe irritation (reddening, inflammation), maceration (whitening of the skin), hypergranulation (excess tissue formation) or sensitivity (allergic reaction) consult a health care professional.
Frequent dressing changes on wounds with damaged or delicate skin surrounding the wound is not recommended. The wound should be inspected during dressing changes. Contact a health care professional if (1) signs of infection occur (increased pain, bleeding, wound drainage), (2) there is a change in wound color and/or odor, (3) the wound does not begin to show signs of healing and (4) any other unexpected symptoms occur.
The dressing may be used on infected wounds only under the care of a health care professional.
The use of this device neither guarantees nor warrantees against AIDS transmission.
In addition, for leg ulcers (venous stasis ulcers, arterial ulcers and leg ulcers of mixed etiology), diabetic ulcers, pressure ulcers, burns (first- and second-degree), surgical wounds and traumatic wounds:

• Treatment of the above wound types should be under the supervision of a health care professional.
• Appropriate supportive measures should be taken where indicated (e.g., use of graduated compression bandaging in the management of venous leg ulcers or pressure relief measures in the management of pressure ulcers).
• Colonization of chronic wounds is common and is not a contraindication to the use of the dressing. The dressing may be used on infected wounds under medical supervision together with appropriate therapy and frequent monitoring of the wound. In the presence of a clinical anaerobic infection, occlusive therapy is not recommended.
• The control of blood glucose, as well as, appropriate supportive measures should be provided with diabetic foot ulcers.

Store at room temperature. Avoid refrigeration and exposure to high humidity.