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Nanova Therapy System

The Nanova Therapy System is a compact, manually activated single-patient use Therapy Unit that is coupled to an absorptive Dressing to form a Negative Pressure Wound Therapy System suitable for use on shallow-cavity chronic and acute wounds.

Nanova Therapy System

Therapy Unit

The Nanova Therapy Unit has been designed with both care giver and patient in mind.

  • Manual priming – no complicated training required.
  • 1–3 compressions of the pump delivers regulated negative pressure that can be re-primed at any time.
  • Once activated, negative pressure is maintained at -125 mmHg.
  • Single-patient use Therapy Unit can be used with multiple dressings as required for up to 30 days.
  • Silent, light-weight and small; can easily be carried in a pocket.

Nanova Therapy System


The Nanova Dressing delivers negative pressure to the wound bed whilst absorbing and locking away wound exudate. The dressing has a silicone wound contact layer that is designed to be non-adherent. The adhesive border features DermaTac Protective Seal Technology, this a hybrid material combining silicone and acrylic adhesives that provide an effective seal for negative pressure, yet enables easy repositioning or removal minimising trauma to the peri-wound skin.

  • Wound fluid is locked within the core of the dressing to help minimise the potential for maceration.
  • Continues to absorb exudates if negative pressure is lost.
  • Dressing may be placed in any orientation without compromising absorptive capacity or the delivery of negative pressure.


The Nanova Therapy System is indicated for patients who would benefit from wound management via the application of negative pressure, particularly as the device may promote wound healing through the removal of excess exudates and infectious materials

The Nanova Therapy System is indicated for removal of small amounts of exudate from chronic, acute, traumatic, subacute and dehisced wounds, partial-thickness burns, ulcers (such as diabetic, venous or pressure), surgically closed incisions, flaps and grafts.


•• The Nanova Therapy System is contraindicated for patients with:

  • Malignancy in the wound
  • Untreated osteomyelitis
    Note: Refer to Warnings section for information concerning osteomyelitis.
  • Non-enteric and unexplored fistulas
  • Necrotic tissue with eschar present
    Note: After debridement of necrotic tissue and complete removal of eschar, Nanova Therapy may be used.
  • exposed vasculature
  • exposed nerves
  • exposed anestomatic site
  • exposed bone or tendons



Dimensions (Therapy Unit)4.7cm x 10.0cm (1.85 in D x 3.94 in H)
Weight (Therapy Unit)0.072kg (0.16 lb)
Pressure-125 mmHg (16.6 kPa)
Therapy Delivery ModeContinuous
Dressing Absorbency Capacity>40 ml
Storage Conditions
Temperature Range-18° C (0° F) to 60° C (140° F)
Relative Humidity Range0 - 90% non-condensing
Operating Conditions
Temperature Range5° C (41° F) to 40° C (104° F)
Relative Humidity Range15 - 93% non-condensing
Atmospheric Pressure1060 hpa (-1253ft/-381.9m) to 700 hpa (9878ft/3010m)
Expected Service Life of Nanova Therapy Unit30 Days

Ordering information

Nanova Therapy System Starter Kit

Each starter kit includes;
1 x Therapy Unit
2 x Absorptive Dressings 18cm x 18cm
2 x Optional use GranuFoam® 8.0cm x 8.0cm, 6.0mm thick

Nanova Dressing Pack

Each dressing pack contains;
3 x Absorptive Dressings 18cm x 18cm
3 x Optional use GranuFoam® 8.0cm x 8.0cm, 6.0mm thick

Note: Nanova Starter and Dressing Kits are supplied in cartons of three kits each. As ordering codes may vary between countries please contact KCI office.

Important Message for Patients

The information on this site is intended for healthcare professionals. Patients should consult with their healthcare professional providers regarding their specific medical conditions and treatments as well as the information provided on this site, including the risks and benefits of certain products and services that may be discussed on this site.

For more information on Nanova Therapy and other KCI products, click here.

Important Safety Information and IFU

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