ZeniFOAM Gentle Border

ZeniFOAM Gentle Border is a sterile, multi-layered, absorbent polyurethane foam dressing with a silicone adhesive border. The dressing is designed to absorb 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 and prevents drainage strike-through.

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

• Multi-layered high performance dressing
• Highly absorbent
• Available in anatomical shapes
• Non-adherent to wound bed
• Lint free, no particulates left in wound
• Protects against maceration
• Can be repositioned after application
• Gentle on sensitive, fragile skin
• Used as primary or secondary dressing
• Highly conformable and comfortable
• Waterproof backing
• Easy application and removal
• May be used in pressure reduction/protection protocols

Indications

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

Contraindications

• Full-thickness (third-degree) burns
• Dry or necrotic wounds without exudate, unless used with topical gel/ointment.
• Patients with known hypersensitivity tor allergy to polyurethane foam, silicone or any component of the dressing.

Warnings and Precautions

• Single patient use only. Do not reuse.
• Application of lotions or ointments to the peri-wound skin may reduce adherence of the silicone border.
• If signs of irritation or sensitization occur, discontinue use.
• Do not use with oxidizing agents (e.g., hydrogen peroxide, hypochlorite solutions) which may degrade the dressing.

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.

How Supplied/Sizing
2"x2", 3"x3", 4"x4", 6"x6", 7"x7" Sacral, 9"x9" Sacral, 5.5"x5" Heel, 10"x9.4" Heel
HCPCS Code
Product features
check_circle Adhesive border
check_circle Antimicrobial format available
check_circle Compatible w/ topicals
check_circle Cuttable
check_circle Flexible
check_circle Intact when saturated
check_circle Moisture vapor permeable
cancel Odor-reducing
check_circle One-piece removal
check_circle Pressure redistribution
cancel Secondary dressing required
check_circle Self-adhering
check_circle Silicone-based adhesive
cancel Surfactant impregnated
check_circle Usable on infected wounds
check_circle Variety of sizes
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
May be used to skin pressure reduction/protection protocols to reduce friction, provide waterproof
breathable barrier and abrasion protection

Mode of Use/Application

1. Cleanse the wound according to clinical practice.
2. Gently dry the surrounding skin.
3. Select a dressing with a pad size that extends at least one inch beyond the wound margin.
4. Remove the release liners and apply with the silicone contact layer facing the wound bed.
5. Smooth the silicone adhesive border onto the surrounding skin to secure.

Removal & Change Frequency

1. When the exudate approaches the edge of the dressing; when the border is no longer intact with the skin; or per institutional protocol. Wear time per dressing should not exceed more than 7 days.
2. To remove, gently lift one corner and peel back carefully.

Construction

• Semi-permeable polyurethane film backing
• Super absorbent core
• Non-woven layer
• Polyurethane foam pad
• Meshed silicone contact layer and border
• Latex free

Clinically Tested

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

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