Supra SDRM®

The Supra SDRM^® device is indicated for use in the management of partial- and full-thickness wounds, pressure injuries (stage 1 and 4), venous ulcers, ulcers caused by mixed vascular etiologies, venous stasis and diabetic ulcers, first- and second-degree burns, partial-thickness burns, cuts, abrasions, acute wounds, trauma wounds, surgical wounds, superficial wounds, and grafted wounds and donor sites.

Contraindicated for use in the presence of active infection.

DO NOT USE in procedures where permanent coverings are required.
These biodegradable devices provide temporary covering and are not intended as permanent coverings.
Discard and DO NOT USE previously opened or damaged devices and use only devices that are packaged in unopened and undamaged containers.
DO NOT USE if there is loss of sterility of the device.
DO NOT RE-STERILIZE. DO NOT USE beyond expiration date.
FOR SINGLE USE ONLY. DO NOT RE-USE.
Discard any unused portions of the product once the package is opened.
DO NOT USE on wounds with excessive bleeding without the use of additional hemostatic treatment.
ALWAYS clean and debride the wound before applying Supra SDRM^®.
The use of antiseptic solution should be used for deeper and more severe wounds.
DO NOT expose Supra SDRM^® to excessive temperatures.
Be sure to discard the GREEN PAPER surrounding SupraSDRM^®. Supra SDRM^® does NOT have unique sides.
Either side of Supra SDRM^® may be applied against the wound.
Supra SDRM^® should be removed if there is an active infection or in cases where there is severe pain or accumulations of wound secretions.
Supra SDRM^® should be removed immediately if there are any signs of allergic reaction to the material.

The following complications are possible. If any of these conditions occur, the device should be removed.
• Infection
• Chronic inflammation
• Allergic reaction