ZeniFOAM-Ag Gentle Border

ZeniFOAM-Ag Gentle Border is a sterile, nonadherent, absorbent polyurethane foam dressing containing ionic silver and a silicone adhesive border. The dressing is designed to absorbs moderate to heavy exudate and help maintain a moist wound environment. The multi-layered construction supports cushioning protection, fluid management, reduces the risk of peri-wound maceration, and allows secure placement with atraumatic removal. The semi-permeable film backing provides a barrier to external contaminants while allowing moisture vapor transmission, and the silicone adhesive border secures the dressing in place. Each dressing contains 0.25–0.35 mg/cm3 ionic silver, which provides antibacterial activity for up to 7 days in vitro.

Focus Health Group

Since 2002, Focus Health Group has grown into a health services company providing pharmaceutical products and a complete line of advanced wound care dressings with the mission to provide quality, effective wound care products to aid in the delivery of optimal patient care and outcomes.

Website: https://www.focushealthgroup.com
Benefits

• Broad spectrum antimicrobial
• Antimicrobial effectiveness up to 7 days
• Highly Absorbent
• Silicone adhesive border
• Protects against maceration
• Can be repositioned after application
• Gentle silicone layer for sensitive, fragile skin
• Non-adherent to wound bed
• Highly conformable and comfortable
• May be cut to size/shape
• Waterproof backing
• Easy application and removal
• Used as a primary or secondary dressing

Indications

ZeniFOAM-Ag Gentle Border is indicated for the management of moderate to heavily exuding wounds, including:
• Pressure injuries
• Venous leg ulcers
• Diabetic foot ulcers
• Surgical wounds
• First- and second-degree burns
• Donor sites
• Superficial
• Partial thickness
• Traumatic wounds (lacerations, abrasions, skin tears).

Contraindications

ZeniFOAM-Ag Gentle is contraindicated for:
• Full-thickness (third-degree) burns
• Dry or necrotic wounds without exudate
• Patients with known hypersensitivity or allergy to silver, polyurethane foam, silicone, or any dressing component.

Warnings and Precautions

• Single patient use only. Do not reuse.
• ZeniFOAM-Ag Gentle Border does not replace systemic therapy or other appropriate infection management for clinically infected wounds.
• Application of lotions or ointments to the peri-wound skin may reduce adherence of the silicone border.
• Do not use with oxidizing agents (e.g., hydrogen peroxide, hypochlorite solutions) as these may degrade the dressing.
• ZeniFOAM-Ag Gentle Border is intended for short-term use and should not be used for durations longer than 28 days. Transient discoloration of the wound or surrounding skin may occur. Prolonged or repeated use may cause permanent skin discoloration.
• Remove the dressing prior to diagnostic procedures or treatments involving MRI, radiation therapy, X-ray, ultrasound, thermotherapy or microwave diathermy.
• Avoid contact with electrodes or conductive gels during electronic measures such as electrocardiogram (ECG) and electroencephalograms (EEG).
• If skin reddening or sensitization occurs, discontinue use.

Adverse Effects/Reactions

No known adverse effects/reactions.

Storage Requirements

Store at room temperature in a cool, dry place. Avoid direct sunlight and excessive humidity. Dispose of used dressing per institutional policy and local regulations.

Active Ingredients

Ionic silver

How Supplied/Sizing
4"x4", 6"x6"
HCPCS Code
Product features
cancel Absorptive dressing format
cancel Alginate dressing format
cancel Antimicrobial effects up to 48 hours
cancel Antimicrobial effects up to 3 days
check_circle Antimicrobial effects up to 7 days
cancel Bacterial binding
cancel Bacterial trapping
cancel Bactericidal
check_circle Bactericidal broad-spectrum
check_circle Bacteriostatic
cancel Collagen dressing format
cancel Composite dressing format
cancel Contact layer dressing format
check_circle Foam dressing format
check_circle Fungicidal
cancel Gauze or non-woven dressing format
cancel Gelling fiber dressing format
cancel Hydrogel (amorphous) dressing format
cancel Hydrogel (impregnated) dressing format
cancel Hydrogel (sheet) dressing format
check_circle Impermeable to outside contaminants
cancel Impregnated dressing format
cancel Microbicidal
check_circle Moisture vapor permeable
cancel Secondary dressing required
check_circle Silicone-based adhesive
cancel Sporicidal
cancel Super absorbent polymers
check_circle Sustained release formula
cancel Transparent film dressing format
cancel Virucidal
cancel Wound filler dressing format
Other features
check_circle Educational Material Available
check_circle Free Samples/Trials Available
cancel Published Clinical Article Available
Recommended Use

Acute Wounds
Burns
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
Granulating/Epithelializing Wounds
Infected Wounds
Moderate/Highly Exudating Wounds
Palliative Wounds
Pressure Ulcers
Sloughy Wounds
Superficial Wounds
Surgical Wounds
Venous Ulcers

Mode of Use/Application

1. Cleanse the wound per institutional protocol.
2. Gently dry the surrounding skin.
3. Select a dressing size that extends at least 1 inch beyond the wound margin. The dressing may be cut to fit the wound size and shape, if required.
4. Remove the release liners and apply the silicone contact surface directly to the wound bed.
5. Smooth the silicone adhesive border onto the surrounding skin to secure.

Removal & Change Frequency

1. Change the dressing based on wound condition and exudate level. Replace every other day; when the exudate reaches the dressing edge, when the border is no longer intact with the skin; or per healthcare provider instructions. Wear time per dressing should not exceed more than 7 days.
2. To remove, gently lift one edge and slowly peel back.

Construction

• Polyurethane foam pad containing silver
• Semi-permeable polyurethane film backing
• Meshed silicone contact layer
• Latex free

Clinically Tested

Latex-friendly
Non-allergenic
Non-cytotoxic
Non-irritating

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