Additional Advanced Dressing

Silicone Wound Contact layer

Silicone wound contact layer dressing with box

About Kliniderm® Silicone Wound Contact Layer

Kliniderm® Silicone Wound Contact Layer is a transparent, flexible wound dressing. The soft silicone does not stick to the wound surface and reduces trauma to delicate new tissue upon removal. The Kliniderm® Silicone Contact Layer consists of 3 layers: a PET film, a polyurethane net that is one-side coated with a soft silicone and a release film. The middle layer is the functional component and the coated surface should contact the wound. The porous structure of the wound contact layer allows exudate to pass into a secondary absorbent dressing. The wound contact layer prevents the secondary dressing from sticking to the wound and ensures atraumatic dressing changes. The wound contact layer seals around the wound edges, preventing the exudate from leaking onto the surrounding skin, thus minimizing the risk of maceration. High transparency allows wound inspection during application and wear.

Not made with natural rubber latex or DEHP. Medical device.

Product benefits

  • Porous structure allowing exudate to pass into a secondary dressing
  • High transparency allows wound inspection during application and wear
  • Seals around the wound edges, preventing the exudate from leaking onto the surrounding skin, thus minimizing risk of maceration
  • Does not stick to the wound surface
  • Can remain in place for up to 14 days

Indications

Kliniderm® Silicone Wound Contact Layer is indicated for use in combination with a secondary absorbent dressing on a wide range of exuding wounds, such as:

  • Diabetic foot ulcers
  • Pressure ulcers
  • Leg (venous and arterial) ulcers
  • First- and second-degree burns
  • Surgical wounds
  • Traumatic wounds
  • It can also be used as wound protective layer on non-exuding wounds and on areas with fragile skin. 

Contra-Indications

  • Do not use on third-degree burns.
Downloads

Download here some more product information about Kliniderm® Silicone Wound Contact Layer.

Directions for use

Application

  1. Clean the wound area according to good wound care practice. Ensure the peri-wound skin is dry.
  2. Select a suitable size of Kliniderm® Silicone Wound Contact Layer so that the dressing overlaps the wound margins by at least 1 cm. Large wounds may require more overlap. The product may be cut to size with the backing paper still on.
  3. Remove the release film and gently apply the wound contact layer directly on the wound surface; peel-off the dressing carrier and smooth down the dressings edges to ensure good adhesion.
  4. Apply an appropriate secondary absorbent dressing and a retention dressing if needed.

Dressing change and removal

  1. Kliniderm® Silicone Wound Contact Layer can remain in place for up to 14 days, dependent on the condition of the patient and clinical condition of the wound. The longest cumulative use should be less than 30 days.
  2.  Replace Kliniderm® Silicone Wound Contact Layer whenever good wound care practice dictates that the dressing should be changed.
  3. Gently remove the dressing from the wound bed and skin (by supporting surrounding skin) and dispose according to local procedures and guidelines. If removal appears to be difficult, saturate the dressing with saline solution.
  4. If required, irrigate the wound site according to good wound care practice.
  5. If the condition of the wound deteriorates, discontinue use.

Precautions

  • In case of signs of infection, consult a health care professional for adequate infection treatment.
  • Do not use on patients with a known sensitivity to silicone, PET film or polyurethane.
  • Sterile if pouch and seal are intact. Do not use if damaged.
  • Do not re-use. Re-use can cause serious infections.
  • Do not re-sterilize.
  • For external use only.
  • For use under the guidance of a healthcare professional.

Storage

The products should be stored under ambient conditions, in the original packaging. In a cool, dry and well ventilated place, away from direct sunlight.

In case a serious incident has occurred in relation to the device: Inform Medeco BV as listed on the packaging, your local distributor and your local healthcare authority.

Last update: Revision 16-01-2025