ZeniCONTACT is a sterile, transparent, meshed silicone contact layer designed to protect the wound bed and allow exudate to pass through into a secondary dressing. The silicone is gentle and non-adherent to the wound to prevent secondary dressings from adhering to fragile tissue and minimizes trauma during dressing changes.
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.
• Open meshed, 2 sided, silicone contact layer
• Conforms easily
• Flexible and soft
• Allows exudate to pass through to secondary dressing
• Gentle, non-adherent to wound bed
• Can be cut to size/shape
• Prevent secondary dressings from adhering to wound bed
• Used as primary dressing
• Approved for use with NPWT or as topical ointment carrier
ZeniCONTACT is indicated for use as a wound contact layer in conjunction with appropriate secondary dressings. It may also be used as a topical ointment carrier or with negative pressure wound therapy (NPWT). Indications include:
• Skin tears
• Donor sites
• Partial-thickness burns
• Blisters
• Skin grafts
• Chronic wounds requiring a gentle protective interface.
Do not use ZeniCONTACT as a stand-alone dressing. Contraindicated in patients with known hypersensitivity or allergy to silicone. For skin grafts, skin tears or blister protection, avoid lifting or removing ZeniCONTACT within 5 days post-application to prevent wound disturbance.
• Single patient use only. Do not reuse.
• Requires a secondary dressing appropriate for exudate levels.
• 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.
• Silicone is naturally sticky to the touch; however, when in contact with wound drainage or moisture, the silicone loses adherence.
No known adverse effects or reactions.
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.
Acute Wounds
Burns
Cavity Wounds
Chronic Wounds
Deep Wounds
Dehisced Wounds
Diabetic Foot
Granulating/Epithelializing Wounds
Hypertrophic Scars/Keloids
Infected Wounds
Moderate/Highly Exudating Wounds
Non/Minimally Exudating Wounds
Palliative Wounds
Pressure Ulcers
Sloughy Wounds
Superficial Wounds
Surgical Wounds
Venous Ulcers
In conjunction with NPWT
1. Cleanse the wound according to clinical practice.
2. Gently dry the surrounding skin.
3. ZeniCONTACT may be cut to size and shape, if necessary, to cover the wound with at least one inch beyond the wound margin.
4. ZeniCONTACT is packaged with a release liner on both sides of the dressing. Remove the first release liner to expose the silicone and place the silicone side touching the wound bed. Then, remove the second release liner.
5. Secure with an appropriate absorbent secondary dressing.
1. Change frequency depends on wound condition and exudate level. Replace the dressing per healthcare provider instructions. When using on skin grafts, skin tears or protection of blisters, do not lift or remove ZeniCONTACT prior to 5 days post-application to prevent wound disturbance. Irrigate the wound with sterile water or saline to loosen adherence, if necessary. Wear time per dressing should not exceed more than 7 days.
2. To remove, gently lift one corner and peel back carefully.
Secure in place with appropriate secondary dressing such as a foam, composite, gauze or with negative pressure wound therapy.
• Soft silicone mesh
• Latex free
Latex-friendly
Non-allergenic
Non-cytotoxic
Non-irritating
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