Therabond® 3D Antimicrobial Systems with Silvertrak™ Technology
Therabond® 3D Antimicrobial Systems are absorbent, post-operative dressings consisting of silver-plated nylon three-dimensional fabric. Provides an effective barrier to bacterial penetration for up to 14 days. In the presence of exudate, the dressing will help maintain a moist wound environment.
Argentum Medical, LLC
Argentum Medical, LLC is the manufacturer of the Silverlon™ family of advanced seven day use antimicrobial metallic silver burn, wound, surgical, negative pressure and IV catheter dressings.Benefits
• Kills pathogens on contact
• Achieves 99.99% reduction of pathogens at 15 minutes
• Proven broad spectrum antimicrobial protection for up to 14 days
• Kills a broad range of pathogens including MRSA and VRE
• Promotes an optimal healing environment
• Actively transports excess fluid and exudate (cellular debris) away from the wound
• Controls maceration and bioburden
• Fewer dressing changes
• Durable, flexible material adapts to the patient's anatomy and the wound
• Soft, silver nylon material breathes and moves with the patient to minimize friction
• Provides gentle compression
• Enhances patient comfort
• Non-staining
• Easy to apply
Indications
TheraBond®3D is indicated for use in light to moderately exuding partial- and full-thickness wounds including traumatic wounds, surgical wounds, donor sites, first- and second-degree burns, as well as pressure ulcers, diabetic ulcers and vascular ulcers. TheraBond®3D may be used over debrided and partial-thickness wounds.
Contraindications
Do not use on patients with a known sensitivity to silver.
Do not use on patients during MRI (Magnetic Resonance Imaging) examination.
Prior to commencing radiation therapy, remove TheraBond®3D. Apply a new TheraBond®3D Antimicrobial Barrier System following treatment.
Warnings and Precautions
For external use only.
TheraBond®3D is not compatible with oil-based products such as petrolatum.
TheraBond®3D may not be compatible with topical antimicrobials.
Do not use TheraBond®3D with saline solutions or povidone iodine.
Avoid contact with electrodes or conductive gels during electronic measurements e.g. EEG and ECG.
TheraBond®3D is not intended to provide treatment for infected wounds.
TheraBond®3D may be used on infected wounds which are being managed in accordance with institutional clinical protocols for infection abatement as an adjunct to the standard treatment regimen to provide a barrier to bacterial infection.
If reddening or sensitization of the skin occurs, discontinue use.
TheraBond®3D should only be used in premature infants (less than or equal to 37 weeks gestation) when clinical benefit outweighs any potential patient risks.
Storage Requirements
Store at room temperature.
Active Ingredients
Silver, 15% by weight
Inactive Ingredients
Nylon
How Supplied/Sizing
Contact: 1(1/2)"x6", 1(1/2)"x10", 4(1/2)"x4(1/4)", 4"x8", 8"x16", 24"x24". Wraps: 4"x72", 6"x96". Island: 2"x2", 4"x5", 4"x6", 4"x8", 4"x10", 4"x12". Island-XS: 4"x10", 4"x14". Gloves: Medium, large, x-large.
Product features
Absorptive dressing format
Alginate dressing format
Antimicrobial effects up to 48 hours
Antimicrobial effects up to 3 days
Antimicrobial effects up to 7 days
Bacterial binding
Bacterial trapping
Bactericidal
Bactericidal broad-spectrum
Bacteriostatic
Collagen dressing format
Composite dressing format
Contact layer dressing format
Foam dressing format
Fungicidal
Gauze or non-woven dressing format
Gelling fiber dressing format
Hydrogel (amorphous) dressing format
Hydrogel (impregnated) dressing format
Hydrogel (sheet) dressing format
Impermeable to outside contaminants
Impregnated dressing format
Microbicidal
Moisture vapor permeable
Secondary dressing required
Silicone-based adhesive
Sporicidal
Super absorbent polymers
Sustained release formula
Transparent film dressing format
Virucidal
Wound filler dressing format
Other features
Educational Material Available
Free Samples/Trials Available
Published Clinical Article Available
Recommended Use
Acute Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
First- and Second-Degree Burns
Granulating/Epithelializing Wounds
Infected Wounds
Moderate/Highly Exuding Wounds
Non/Minimally Exuding Wounds
Palliative Wounds
Pressure Ulcers
Sloughy Wounds
Superficial Wounds
Surgical Wounds
Traumatic Wounds
Venous Ulcers
Mode of Use/Application
Island Systems:
Cleanse wound with sterile water. Choose a system where the pad completely covers the wound. Remove system from sterile pouch, using aseptic technique.
To apply: remove half of the release paper and place silver pad in contact with the wound. Remove second half of the release paper and smooth system down.
To remove: lift one corner and slowly remove in a motion parallel to the skin. Dressing should be changed based on the amount of exudate or the condition of the wound.
Note: The system may adhere on wounds that are dry or have very light exudate. If the system is not easily removed, then moisten or soak to assist removal.
Wraps and Contact Systems:
Cleanse wound with sterile water. Choose a system that completely covers the wound. Remove system from sterile pouch, using aseptic technique.
To apply: moisten the system with sterile water and place the textured side in contact with the wound. Cover and secure the system periwound care protocol.
To remove: lift one corner and slowly remove in a motion parallel to the skin. Dressing should be changed based on the amount of exudate or the condition of the wound.
Note: The system may adhere on wounds that are dry or have very light exudate. If the system is not easily removed, then moisten or soak to assist removal.
Removal & Change Frequency
Dressing should be changed based on the amount of exudate or the condition of the wound.
Additional Recommended Dressings
Contact and wrap dressings should be used in conjunction with an outer absorbent dressing.
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