AQUACEL® Ag Surgical SP dressing is a sterile post‐operative dressing comprising an inner non‐woven pad made of Hydrofiber® Technology and ionic silver. The pad is composed of a hydrocolloid adhesive (top layer) bound to an outer polyurethane film and a windowed polyurethane film skin contact layer, placed between one layer of acrylic and one layer of hydrocolloid contacting the skin.
• Comfortable and flexible
• Slim profile design
• Waterproof
• Cover layer of polyurethane film provides a waterproof viral and bacterial barrier
AQUACEL® Ag Surgical SP may be used for the management of wounds healing by primary intent and as an effective barrier to bacterial penetration, to help reduce infection.
The following adverse reactions have been identified during use of AQUACEL® Ag Advantage SURGICAL cover dressings or their components:
• Skin irritation/rash/mucosal irritation
• Allergic response (localized)
• Mild pain/discomfort
• Superficial tissue damage
• Delayed healing/abnormal scarring of wound
Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or establish a causal relationship to AQUACEL® Ag SURGICAL SP cover dressings exposure. The absolute number of adverse events is unknown but believed to be very low. Such events are generally transitory in nature and should resolve shortly after discontinuing treatment with the dressing. Should symptoms persist or worsen, please seek medical advice.
This product is for single use only and is supplied sterile. If the inner package is damaged, do not use the dressing. Store at room temperature (10°C–25°C/50°F–77°F). Keep dry.
Acute Wounds
Dehisced Wounds
Infected Wounds
Surgical Wounds
Non/Minimally Exudating Wounds
Initially remove 3/4 of the backing film along the length of the dressing minimizing finger contact with the central pad and the adhesive surface. Place at one side of the wound/incision line. Gently roll the dressing over the wound/incision line and mold into place.
Remove the remaining 1/4 backing film and gently mold the dressing in place with hand for a secure adhesion. Do not stretch. The translucent hydrocolloid backing allows the clinician to monitor the central Hydrofiber™ pad and assess when the dressing needs to be changed. The dressing can be left in place for up to 7 days subject to regular clinical assessment.
To remove the dressing, press down on the skin with one hand and carefully lift an edge of the dressing with other hand. Stretch the dressing to break the adhesive seal and remove.
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