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SUPRA SDRM®

SUPRA SDRM® is an absorbable, micro-porous biodegradable matrix indicated for the management of superficial dermal wounds, split-skin graft donor sites, pressure and venous ulcers, and second-degree burns.

PolyMedics Innovations Inc.

PolyMedics Innovations (PMI) specializes in innovative biomaterials for the effective treatment of wounds, featuring SUPRA SDRM®: an optimized and proven wound closure matrix to manage chronic and difficult-to-heal wounds.
Fax:(646) 350-3129 Website: polymedics.com/us/
Benefits

SUPRA SDRM® combines the benefits of the microporous structure found in SUPRATHEL® – which creates a protective barrier allowing the wound to heal – with additional larger pores that enable ingrowth of blood vessels needed to manage chronic and difficult-to-heal wounds.

Indications

The SUPRA SDRM® device is indicated
for use in the management of:
• Partial and full thickness wounds
• Pressure (stage I and IV) and venous ulcers
• Ulcers caused by mixed vascular etiologies
• Venous stasis and diabetic ulcers
• 1st and 2nd degree burns
• Partial thickness burns
• Cuts and abrasions
• Acute wounds
• Trauma wounds
• Surgical wounds
• Superficial wounds
• Grafted wounds and donor sites

Contraindications

Active infection

Warnings and Precautions

• DO NOT USE in procedures where permanent coverings are required. These biodegradable devices provide temporary covering and are not intended 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 SUPRA SDRM®.
• 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.

Adverse Effects/Reactions

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

Storage Requirements

Use only if sterilization indicator is red. Store at -20°C to 25°C (-4°F to 77°F). Keep away from heat sources.

How Supplied/Sizing
2cmx2cm, 5.1cmx5.1cm, 9cmx9cm, 9cmx12cm, 18cmx9cm, 18cmx18cm, 18mm.
HCPCS Code
Product features
cancel Biosynthetic
cancel Biosynthetic: animal-based
check_circle Indicated for chronic vascular ulcers
check_circle Indicated for diabetic ulcers
cancel Indicated for draining wounds
check_circle Indicated for partial- and full-thickness wounds
check_circle Indicated for pressure ulcers
check_circle Indicated for surgical wounds
cancel Indicated for third-degree burns
check_circle Indicated for trauma wounds
check_circle Indicated for venous ulcers
check_circle Synthetic
check_circle Variety of sizes
check_circle Resorbable
cancel Contact manufacturer for usage guidelines
Other features
check_circle Educational Material Available
check_circle Free Samples/Trials Available
check_circle Published Clinical Article Available
Recommended Use

Acute Wounds
1st and 2nd Degree Burns
Cavity Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
Palliative Wounds
Pressure Ulcers
Superficial Wounds
Surgical Wounds
Traumatic Wounds
Venous Ulcers

Clinically Tested

Non-cytotoxic
Non-irritating
Non-sensitizing

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