Invia® NPWT Foam Dressing Kits contain hydrophobic reticulated polyurethane foam with large open-cell structure intended to help promote wound healing. Use with Invia® NPWT systems.
The Invia® Foam Dressing Kit with FitPad in conjunction with the Invia Motion® and Invia® Liberty™ Negative Pressure Wound Therapy (NPWT) Systems is indicated for patients who would benefit from a suction device (negative pressure wound therapy) as when used on open wounds it creates an environment that promotes wound healing by secondary or tertiary (delayed primary) intention by preparing the wound bed for closure, reducing edema, promoting granulation tissue formation and perfusion, and by removing exudate and infectious material. When used on closed surgical incisions, the Invia® Foam Dressing Kit with FitPad is also intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.
Invia® Foam Dressing Kits are indicated for use on: acute or sub-acute wounds, chronic wounds, dehisced wounds, pressure injuries, diabetic/neuropathic ulcers, venous insufficiency ulcers, traumatic wounds, partial-thickness burns, flaps and grafts, and closed surgical incisions.
Invia® NPWT Foam Dressing Kits are contraindicated in the presence of: necrotic tissue with eschar present, untreated osteomyelitis, non-enteric and unexplored fistulas, in wound (with exception of palliative care to enhance quality of life), exposed vasculature, exposed nerves, exposed anastomotic site of blood vessels or bypasses, or exposed organs.
Granulating/ Epithelializing Wounds
Moderate/Highly Exudating Wounds
To apply, use clean/aseptic or sterile technique in accordance with institution protocol. The Invia® NPWT Foam Dressing Kit is only to be used by qualified and trained personnel. Dressings should be changed every 48 to 72 hours but no fewer than 3 times a week or as instructed by a clinician. The frequency of dressing changes should be based on an evaluation of the wound condition rather than standard recommendations.
Kits contain wound foam (available in three sizes), external suction interface (ESI), and transparent film. Neither the dressing kit nor the packaging contains natural rubber latex.
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