Description
Class IIb device.
Non-adherent polyethylene dressing impregnated with the patented L-Mesitran Soft gel which contains: 40% medical grade honey, medical grade hypoallergenic lanolin (Medilan), propylene glycol, PEG 4000 and vitamins C & E.
When the gel comes into contact with the wound, fluid is drawn from the surrounding tissues. In this way, a moist environment is created for wound healing. This environment stimulates the wound healing process: by facilitating the autolysis of necrotic and other devitalized material, it helps the preparation of the wound bed and promotes better migration of epithelial cells .
- Thanks to the strong osmotic activity, L-Mesitran Tulle has antibacterial properties.
- The gel will gradually dilute and can be removed easily according to local wound cleansing protocols.
- L-Mesitran Tulle is a primary wound dressing which should be covered with secondary dressings deemed appropriate.
- Being produced with natural ingredients, each batch of gel can vary in color (white - yellow - brown), maintaining its properties unchanged.
- The gel may contain visible sugar crystals; however, this will not affect the effectiveness and/or application of the gel.
- The white polyethylene film will allow exudates to pass into the secondary dressing.
Indicated for:
- chronic wounds;
- pressure ulcers (stage I-IV);
- venous stasis ulcers;
- fungal wounds (to help deodorize and/or debride);
- acute colonized wounds;
- surgical wounds;
- postoperative wounds;
- traumatic wounds (superficial wounds, cuts);
- small burns and laser wounds (superficial and partial thickness burns).

Components
Eco-honey, medilan, propylene glycol, PEG 4000 (macrogols), ascorbic acid - vitamin C, vitamin E (DL-alpha-tocopherol acetate), polyethylene film (carrier).

Warnings
It is not suitable for:
- third degree burns;
- patients with a known sensitivity to honey or any other component;
- dirty, infected and heavily exuding wounds (must be cleaned first);
- narrow and deep cavities.
- Due to the low pH of the dressing and high osmolarity, some patients may notice a slight transient burning sensation upon application of the dressing. If burning persists and cannot be managed with a pain reliever, remove dressing, clean area, and discontinue use.
- During initial use of the dressing (depending on the levels of wound exudate, interstitial fluid and edema surrounding the wound), the high osmolarity of the dressing may contribute to increased exudate. This can be managed by adjusting the frequency of dressing changes based on the level of exudate.
- Bacterial colonization in chronic wounds is always present and is not a contraindication to the use of L-Mesitran Tulle.
- During the healing process, due to autolytic debridement, it is normal for non-viable tissue to be removed from the wound resulting in an initial increase in wound size. Although an initial increase in size may be attributed to normal removal of nonviable tissue, seek medical attention if the wound continues to enlarge after the first few dressing changes.
- After removing the dressing, if any material remains on the wound, clean the wound with a solution suitable for the treatment until it can be removed without difficulty.
- Consult a healthcare professional if you notice signs of infection, which may include increased redness, increased pain, increased drainage of the