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AQUACEL FOAM ADHESIVE FORMAT Multi-layered adhesive dressing made of hydrocellular polyurethane foam with a honeycomb structure, accompanied by a thin layer of hydrofibre in contact with the wound bed, an external polyurethane film and a silicone adhesive edge (hypoallergenic). The mixed-cell polyurethane layer is highly hydrophilic, absorbent, exudate-retaining, and breathable. The Hydrofiber Technology layer in direct contact with the wound bed allows AQUACEL Foam to actively interact with the wound, instantly forming a soft gel that maintains a moist environment and retains exudate, promoting healing and reducing the risk of maceration of the periwound skin. The breathable outer film promotes the transmission of vapors and gases and creates an impermeable barrier to fluids and bacteria that protects the wound from external contamination. The silicone adhesive edge is extremely gentle to remove, thin and repositionable. AQUACEL Foam is indicated for use in low to medium exuding wounds on: Traumatic wounds: small abrasions, lacerations, and small cuts. Chronic wounds: leg ulcers (venous ulcers, arterial ulcers and mixed etiology ulcers), diabetic ulcers, partial thickness and full thickness pressure ulcers. Acute wounds: surgical wounds (left to heal by secondary intention) and skin donor sites. Oncological wounds: lesions with high exudate (skin fungal tumors, skin metastases and sarcoma). It can be used as both a primary and secondary dressing. LATEX FREE - PHTHALATES FREE. How to use Choose a dressing of a shape and size such that the central absorbent pad is larger than the wound area. Align the center of the dressing with the center of the wound and place the central pad of the dressing directly over the wound. The dressing should be changed when clinically indicated or when it is saturated with exudate; in any case, no later than after 7 days of dressing in situ. AQUACEL Foam can be used as a primary dressing, or secondary in combination with other products. Components Sterile dressing composed of: an external waterproof polyurethane film, a 2.5 mm thick layer of hydrophilic polyurethane with a density of around 300 g/m2 and a cell size of 200-300 microns, an absorbent layer of non-woven fibres composed of pure sodium carboxymethylcellulose in gelling fibres (NaCMC) surrounded by a thin and delicate silicone adhesive border. Sterilization method: Sterilized by ethylene oxide. Warnings Texttexttext. Please include any warnings/precautions here. Conservation Protect from light, store in a dry place at room temperature (10°C - 25°C). Validity in years: 3. Maximum time spent on site: 7 days. Available codes and presentation/packaging methods Code Measures Units per pack ISO encoding PARAF Code RDM 420804 8x8 cm 10 923590158 1236535/R 420680 10x10 cm 10 09.21.12.003 922859931 1236555/R 420619 12.5x12.5cm 10 922859943 1236556/R 420621 17.5x17.5cm 10 922860059 1236565/R 420623 21x21 cm 5 09.21.12.006 922860061 1236567/R 420624 25x30 cm 5 922860073 1236569/R 420625 20x14 cm-Heel 5 09.21.12.012 922860085 1236571/R 420626 20x17 cm-Sacred 5 09.21.12.012 922860097 1236574/R 420828 24x21.5 cm-Sacred 5 09.21.12.012 926550322 1236575/R 421151 10x20 cm 10 970527990 1377881/R 421153 10x25 cm 10 970528028 1377882/R 421155 10x30 cm 10 970528030 1377885/R Physical characteristics 24-hour exudate management capacity* Total Exudate Handling Capacity (TFHC) 11.00 ± 0.09 g/10 cm²/ 24 hrs Retention and absorption under compression* Absorbency (g/g) 10.71 ± 0.54 Retention (g/g) 8.73 ± 0.29 Withholding percentage 81.6 ± 2.5 Edge thickness (mm) 0.25 Adhesive edge width (cm) 2 cm * Testing was carried out in accordance with BS EN 13726-1:2002 - Test Methods for Primary Wound Dressing Vapor permeability (MVTR) (g/cm 2 ) Absorption capacity (g/cm 2 ) Retention capacity (g/cm 2 ) 24 hours 0.942 0.496 1,439 48 hours 1,914 0.493 2,407 72 hours 2,911 0.493 3,404
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Vânzător: Liki24.co.uk
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