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STERILE DRESSING IN AQUACEL AG FOAM NON-ADHESIVE ABSORBENT HYDROCELLULAR POLYURETHANE FOAM 10X10 CM 10 PIECES

€87,18 €103,20
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CONVATEC ITALIA Srl  |  SKU: 924721879  |  Barcode: 0768455123582


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Description

STERILE DRESSING IN AQUACEL AG FOAM NON-ADHESIVE ABSORBENT HYDROCELLULAR POLYURETHANE FOAM 10X10 CM 10 PIECES



AQUACEL Ag Foam
Non-adhesive format

Description
Multi-layered, non-adhesive, antiseptic cut-to-length dressing made of hydrocellular polyurethane foam with a honeycomb structure, accompanied by a hydrofibre layer in contact with the wound bed with 1.2% by weight of silver ions, a polyurethane binding layer and an external polyurethane film.
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 Ag Foam to actively interact with the wound itself by vertically absorbing the exudate, retaining it and instantly forming a soft gel that maintains the optimal moist environment and promotes healing, reducing the risk of maceration of the perilesional skin, even under compression. The conformability of the gel to the wound bed avoids the presence of empty spaces responsible for bacterial proliferation. The presence of rounded corners prevents the dressing from rolling up. The presence of ionic silver guarantees the dressing a broad-spectrum, rapid and long-lasting antimicrobial activity, without being cytotoxic and irritating. The polyurethane binding layer facilitates the transfer of fluids between the hydrofiber layer and the foam layer, maintains the structure of the dressing even when the dressing is cut and guarantees the removal of a single piece. The breathable external film promotes the permeability of vapors and gases but at the same time creates an impermeable barrier to fluids, viruses and bacteria, protecting the lesion from external contamination.
They are indicated for: lesions with infection or at increased risk of infection; lower limb ulcers; venous stasis ulcers; lower limb ulcers of mixed etiology; arterial ulcers; pressure ulcers; diabetic foot ulcers; surgical wounds; partial thickness burns; traumatic lesions.
They are intended to be used by healthcare professionals, caregivers and patients under the guidance of a healthcare professional.

How to use
Before applying the dressing, clean the wound area with an appropriate wound cleanser and dry the surrounding skin.
Select a dressing size such that the central absorbent pad (area inside the edge of the adhesive window) is 1 cm larger than the wound area. Remove the dressing from the sterile package, avoid touching the surface in contact with the wound. The dressing may be trimmed to size for convenience. Place the dressing over the wound and align the center of the dressing with the center of the wound. Place the pad directly over the wound. Avoid stretching the dressing during application. Ensure that joints are sufficiently loose to allow the patient's mobility. Use a suitable containment bandage or tape to secure the dressing in place if it does not have an adhesive border or if it has been cut. Discard any unused portions of the dressing after placing the dressing on the wound.
The dressing should be replaced when clinically indicated (e.g. leakage, bleeding, increased pain). The maximum recommended application time is 7 days. The wound should be cleaned at appropriate intervals.
To remove the dressing, gently press the skin and carefully lift one corner of the dressing. Continue until all edges are free. Carefully lift the dressing and dispose of according to local clinical protocols. The need for the dressing should be reassessed after 14 days and, where appropriate, an alternative wound management system should be considered.

Components
Sterile dressing composed of an external waterproof polyurethane film, a layer of hydrophilic polyurethane (thickness of 2.5 mm, density of approximately 300 g/m2 and cell size of 200-300 microns), an absorbent layer of pure CMCNa gelling fibres with the addition of 1.2% by weight of silver ions.
Latex free.

Warnings
Sterility of the product is guaranteed if the package is intact and has not been opened before use. Do not use the device if the package is damaged or opened before use. The device must be disposed of in accordance with local regulations.
Dressings are for single use only and should not be reused. Reuse may result in increased risk of infection and cross-contamination and delayed healing.
Although they are water resistant, they should not be immersed in bathing or swimming. They should not be used with other wound care products without first consulting a healthcare professional. They are not compatible with oil-based products. They should not be used on sensitive individuals or those who have had an allergic reaction to the dressing or its components. They are not compatible with oxidizing agents such as hydrogen peroxide or hypochlorite solutions.
Occasionally newly formed blood vessels may produce a wound exudate with traces of blood.
The physician/healthcare professional should be aware that there is a very limited amount of data on the prolonged and repeated use of silver-containing products, particularly in children and neonates. It has been observed that silver-containing products carry a risk of skin discoloration with prolonged use, but this is often transient and resolves once the use of the silver-containing dressing has ceased.
A healthcare professional should be consulted if any of the following conditions are observed during dressing changes: irritation (redness, inflammation), maceration (whitening of the skin), hypergranulation (formation of excess tissue), signs of infection (increased pain, bleeding, warmth/redness of the surrounding tissue, wound exudate) or a change in the color and/or odor of the wound.
After use, the product may represent a potential biological risk. Handle and dispose of the product in accordance with accepted medical practices and applicable national and local laws and regulations. If a serious incident occurs during the use of this device or as a consequence of its use, the incident must be reported to the manufacturer and to the competent authority of the Member State in which the user and/or patient reside.

Conservation
Store in a dry place at room temperature (10°C - 25°C) and protect from light sources.
Validity with intact packaging: 3 years.

Format
Pack of 10 pieces 10 x 10 cm.

Code 420642