Advanced Wound Management Info

Burns

Burn Wounds

A burn is a type of injury to skin, or other tissues, caused by heat, cold, electricity, chemicals, friction, or radiation…. Burns that affect only the superficial skin layers are known as superficial or first-degree burns. They appear red without blisters and pain typically lasts around three days.

Burns are one of the most common household injuries, especially among children. The term “burn” means more than the burning sensation associated with this injury. Burns are characterized by severe skin damage that causes the affected skin cells to die.

Most people can recover from burns without serious health consequences, depending on the cause and degree of injury. More serious burns require immediate emergency medical care to prevent complications and death.

Burn Types

There are three primary types of burns: first-, second-, and third-degree. Each degree is based on the severity of damage to the skin, with first-degree being the most minor and third-degree being the most severe.

Damage includes:

  • First-degree burns: red, nonblistered skin
  • Second-degree burns: blisters and some thickening of the skin
  • Third-degree burns: widespread thickness with a white, leathery appearance
  • Fourth-degree burns: this type of burn includes all of the symptoms of a third-degree burn and also extends beyond the skin into tendons and bones

 

Burns have a variety of causes, including:

  • Scalding from hot, boiling liquids
  • Chemical burns
  • Electrical burns
  • Fires, including flames from matches, candles, and lighters
  • Excessive sun exposure

 

The type of burn is not based on the cause of it. Scalding, for example, can cause all three burns, depending on how hot the liquid is and how long it stays in contact with the skin.

COLLAGEN RECONSRUCTION

INTEGRA DERMAL REGENERATION TEMPLATE DOUBLE LAYER (SKIN)

A two-layer skin regeneration system. The outer layer is made of a thin silicone film that acts as your skin’s epidermis. It protects the wound from infection and controls both heat and moisture loss. The inner layer is constructed of a complex matrix of cross-linked fibres. This porous material acts as a scaffold for regenerating dermal skin cells, which enables the re-growth of a functional dermal layer of skin. Once dermal skin has regenerated, the silicone outer layer is removed and replaced with a thin epidermal skin graft. This completes the procedure and leaves you with flexible, growing skin.

More about Integra® Dermal Regeneration Template Double Layer

INTEGRA DERMAL REGENERATION TEMPLATE SINGLE LAYER (SKIN)

An advanced wound care device comprised of a porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan. The collagen- glycosaminoglycan biodegradable matric provides a scaffold for cellular invasion and capillary growth. It is indicated for the postexcisional treatment of full thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision.

Available in various sizes.

  • IDRT-SL 5cm x 5cm
  • IDRT-SL 10cm x 12,5cm
  • IDRT-SL 10cm x 25cm
  • IDRT-SL 20cm x 25cm

Indications:

INTEGRA® Dermal Regeneration Template is indicated for the postexcisional treatment of full-thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision or not desirable due to the physiological condition of the patient.

INTEGRA® Dermal Regeneration Template is also indicated for use in reconstruction of postexcisional, full-thickness defects of the integument where there is, in the opinion of the treating surgeon, a potential benefit to the patient by improving the reconstructive outcome or decreasing their mortality/morbidity.

More about Integra® Dermal Regeneration Template Single Layer

Integra® Meshed Bilayer Wound Matrix

INTEGRA™ Meshed Bilayer Wound Matrix was specifically designed to be used in conjunction with Negative Pressure Wound Therapy. It is an advanced wound care device comprised of porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan and a semi-permeable polysiloxane (silicone) layer. The meshed bilayer allows drainage of wound exudate and provides a flexible adherent covering for the wound surface. The collagen- glycosaminoglycan biodegradeable matrix provides a scaffold for cellular invasion and capillary growth.

Benefits of INTEGRA™ Meshed Bilayer Wound Matrix include:

  • The consistent meshed design allows better conformity to the wound bed and ease of handling
  • May be used in conjunction with negative pressure wound therapy
  • Allows drainage of wound exudate and provides a flexible, adherent covering for the wound surface
  • Provides immediate wound coverage
  • Highly conformable for various anatomical sites
  • Excellent performance in deep donor sites
  • Room temperature storage
  • Long shelf life
More about Integra® Meshed Double Layer Dermal Regeneration

ReCell®

Activated. Available. Autologous. Complete™

The ReCell® device is used to create a Regenerative Epithelial Suspension – RES™ – which can be used in conjunction with conventional treatments for burns and reconstructive procedures.

ReCell® has been safely used in thousands of procedures worldwide and offers distinct advantages.

  • Definitive Closure with Less Donor Skin
  • Faster epithelialisation of widely-meshed skin graft interstices, decreasing donor skin requirements in mixed depth injuries
  • Smaller donor sites: just 1/80th of the treatment area, for partial thickness injuries like scalds
  • Well suited for large TBSA cases. Can treat up to 1920 cm2

 

Health Economic Benefits:

  • Earlier definitive closure shortens hospital stays
  • Reduced follow-on reconstructive procedures
  • Reduced requirement for scar management
  • Reduced re-admission for closure surgery. Superior Outcomes
  • Regenerated skin has a superior appearance compared with meshed autograft alone
  • Regenerated skin exhibits more normal collagen formation

 

ReCell®:

  • Activated. Available. Autologous. Complete™
More about Recell for Burns Plastics

Flen Pharma Flaminal

Treat 2nd degree burn wounds with Flaminal® Hydro and Forte to achieve excellent results

A convenient wound care solution that leads to good aesthetic and functional results, fulfilling the conditions of an ideal treatment.
Flaminal® Hydro and Forte meet your needs by creating an optimal moisture wound environment, having a continuously debriding effect, protecting against infections and being convenient for the patient and the carer

The versatile, dependable, unique dressing designed to simplify burn care

  • Speeds up healing time
  • Shorter hospital stay
  • Maintains a moist wound environment
  • Continuously debrides the wound
  • Reduces bacteria and controls odour
  • Minimises patient pain and discomfort
  • Non-cytotoxic
  • Hypo-allergenic
  • Easy to apply even in the most difficult areas
  • Cost-effective
  • Can be used at all stages of wound healing
  • Better scar quality
More about Flen Pharma Flaminal

NERVE REPAIR

NeuraGen Nerve Repair

NeuraGen Nerve Guide is an absorbable collagen tube designed to be an interface between the nerve and the surrounding tissue and to create a conduit for axonal growth across a nerve gap.

Available in various sizes:

  • 3cm (length): 1.5mm, 2mm, 3mm, 4mm, 5mm, 6mm & 7mm (Inner Diameter)
  • 2cm (length): 2mm, 3mm, 4mm, 5mm, 6mm & 7mm (Inner Diameter)
More about NeuraGen®

Cavity wounds

Integra® Flowable Wound Matrix

INTEGRA™ Flowable Wound Matrix is an advanced wound care matrix comprised of granulated cross-linked bovine tendon collagen and glycosaminoglycan. The granulated collagen-glycosaminoglycan is hydrated with saline and applied in difficult to access wound sites and tunneled wounds. It provides a scaffold for cellular invasion and capillary growth. When a wound is found to “tunnel” into deep soft tissue and has an irregular geometry, grafting with a sheet form will not be adequate. In order to effectively correct the defect, one must obtain contact with the wound bed and fill the wound. This can be accomplished with INTEGRA™ Flowable Wound Matrix, which is administered through a syringe with a flexible injector. This composition and method of administration allows for complete coverage in deep creviced wounds in a minimally invasive manner.

Benefits of INTEGRA™ Flowable Wound Matrix include:

  • Gel-like consistency allows intimate contact between the grafting material and wound bed
  • Composition and method of administration allows for complete coverage in deep creviced wounds
  • Provides a resorbable scaffold onwhich cells can attach, migrate, proliferate and differentiate
  • Designed with a pore structure that permits cells to migrate into the matrix, allowing them the opportunity to populate and effectively remodel the matrix
  • Indications: INTEGRA™ FlowableWound Matrix is indicated for the management of wounds including: partial and full- thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds, (donor sites/grafts, post-Mohs surgery, post laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears) and draining wounds. The device is intended for one-time use
More about Integra® Flowable Wound Matrix

Venous leg ulcers

COLLAGEN RECONSRUCTION

INTEGRA DERMAL REGENERATION TEMPLATE DOUBLE LAYER (SKIN)

A two-layer skin regeneration system. The outer layer is made of a thin silicone film that acts as your skin’s epidermis. It protects the wound from infection and controls both heat and moisture loss. The inner layer is constructed of a complex matrix of cross-linked fibres. This porous material acts as a scaffold for regenerating dermal skin cells, which enables the re-growth of a functional dermal layer of skin. Once dermal skin has regenerated, the silicone outer layer is removed and replaced with a thin epidermal skin graft. This completes the procedure and leaves you with flexible, growing skin.

More about Integra® Dermal Regeneration Template Double Layer

INTEGRA DERMAL REGENERATION TEMPLATE SINGLE LAYER (SKIN)

An advanced wound care device comprised of a porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan. The collagen- glycosaminoglycan biodegradable matric provides a scaffold for cellular invasion and capillary growth. It is indicated for the postexcisional treatment of full thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision.

Available in various sizes.

  • IDRT-SL 5cm x 5cm
  • IDRT-SL 10cm x 12,5cm
  • IDRT-SL 10cm x 25cm
  • IDRT-SL 20cm x 25cm

Indications:

INTEGRA® Dermal Regeneration Template is indicated for the postexcisional treatment of full-thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision or not desirable due to the physiological condition of the patient.

INTEGRA® Dermal Regeneration Template is also indicated for use in reconstruction of postexcisional, full-thickness defects of the integument where there is, in the opinion of the treating surgeon, a potential benefit to the patient by improving the reconstructive outcome or decreasing their mortality/morbidity.

More about Integra® Dermal Regeneration Template Single Layer

Integra® Meshed Bilayer Wound Matrix

INTEGRA™ Meshed Bilayer Wound Matrix was specifically designed to be used in conjunction with Negative Pressure Wound Therapy. It is an advanced wound care device comprised of porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan and a semi-permeable polysiloxane (silicone) layer. The meshed bilayer allows drainage of wound exudate and provides a flexible adherent covering for the wound surface. The collagen- glycosaminoglycan biodegradeable matrix provides a scaffold for cellular invasion and capillary growth.

Benefits of INTEGRA™ Meshed Bilayer Wound Matrix include:

  • The consistent meshed design allows better conformity to the wound bed and ease of handling
  • May be used in conjunction with negative pressure wound therapy
  • Allows drainage of wound exudate and provides a flexible, adherent covering for the wound surface
  • Provides immediate wound coverage
  • Highly conformable for various anatomical sites
  • Excellent performance in deep donor sites
  • Room temperature storage
  • Long shelf life
More about Integra® Meshed Double Layer Dermal Regeneration

Fibrovein™

Fibrovein™ is a sclerosant used for the treatment of varicose veins. It is a sterile aqueous injection of Sodium Tetradecyl Sulfate (STS), an anionic detergent. It has been used in the treatment of varicose veins since 1946.

FIBROVEIN 3% (S1) H621 (ACT 101/1965), is currently the only strength registered by the Medicines Control Council.
South African Registered Indication: The solution is designed for intravenous use and is used primarily as a sclerosant in the treatment of varicose veins of the leg by compression sclerotherapy.

More about Fibrovein™

Diabetic foot ulcers

INTEGRA DERMAL REGENERATION TEMPLATE DOUBLE LAYER (SKIN)

A two-layer skin regeneration system. The outer layer is made of a thin silicone film that acts as your skin’s epidermis. It protects the wound from infection and controls both heat and moisture loss. The inner layer is constructed of a complex matrix of cross-linked fibres. This porous material acts as a scaffold for regenerating dermal skin cells, which enables the re-growth of a functional dermal layer of skin. Once dermal skin has regenerated, the silicone outer layer is removed and replaced with a thin epidermal skin graft. This completes the procedure and leaves you with flexible, growing skin.

More about Integra® Dermal Regeneration Template Double Layer

INTEGRA DERMAL REGENERATION TEMPLATE SINGLE LAYER (SKIN)

An advanced wound care device comprised of a porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan. The collagen- glycosaminoglycan biodegradable matric provides a scaffold for cellular invasion and capillary growth. It is indicated for the postexcisional treatment of full thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision.

Available in various sizes.

  • IDRT-SL 5cm x 5cm
  • IDRT-SL 10cm x 12,5cm
  • IDRT-SL 10cm x 25cm
  • IDRT-SL 20cm x 25cm

Indications:

INTEGRA® Dermal Regeneration Template is indicated for the postexcisional treatment of full-thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision or not desirable due to the physiological condition of the patient.

INTEGRA® Dermal Regeneration Template is also indicated for use in reconstruction of postexcisional, full-thickness defects of the integument where there is, in the opinion of the treating surgeon, a potential benefit to the patient by improving the reconstructive outcome or decreasing their mortality/morbidity.

More about Integra® Dermal Regeneration Template Single Layer

Integra® Meshed Bilayer Wound Matrix

INTEGRA™ Meshed Bilayer Wound Matrix was specifically designed to be used in conjunction with Negative Pressure Wound Therapy. It is an advanced wound care device comprised of porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan and a semi-permeable polysiloxane (silicone) layer. The meshed bilayer allows drainage of wound exudate and provides a flexible adherent covering for the wound surface. The collagen- glycosaminoglycan biodegradeable matrix provides a scaffold for cellular invasion and capillary growth.

Benefits of INTEGRA™ Meshed Bilayer Wound Matrix include:

  • The consistent meshed design allows better conformity to the wound bed and ease of handling
  • May be used in conjunction with negative pressure wound therapy
  • Allows drainage of wound exudate and provides a flexible, adherent covering for the wound surface
  • Provides immediate wound coverage
  • Highly conformable for various anatomical sites
  • Excellent performance in deep donor sites
  • Room temperature storage
  • Long shelf life
More about Integra® Meshed Double Layer Dermal Regeneration Template

Integra® Flowable Wound Matrix

INTEGRA™ Flowable Wound Matrix is an advanced wound care matrix comprised of granulated cross-linked bovine tendon collagen and glycosaminoglycan. The granulated collagen-glycosaminoglycan is hydrated with saline and applied in difficult to access wound sites and tunneled wounds. It provides a scaffold for cellular invasion and capillary growth. When a wound is found to “tunnel” into deep soft tissue and has an irregular geometry, grafting with a sheet form will not be adequate. In order to effectively correct the defect, one must obtain contact with the wound bed and fill the wound. This can be accomplished with INTEGRA™ Flowable Wound Matrix, which is administered through a syringe with a flexible injector. This composition and method of administration allows for complete coverage in deep creviced wounds in a minimally invasive manner.

Benefits of INTEGRA™ Flowable Wound Matrix include:

  • Gel-like consistency allows intimate contact between the grafting material and wound bed
  • Composition and method of administration allows for complete coverage in deep creviced wounds
  • Provides a resorbable scaffold onwhich cells can attach, migrate, proliferate and differentiate
  • Designed with a pore structure that permits cells to migrate into the matrix, allowing them the opportunity to populate and effectively remodel the matrix
  • Indications: INTEGRA™ FlowableWound Matrix is indicated for the management of wounds including: partial and full- thickness wounds, pressure ulcers, venous ulcers, diabetic ulcers, chronic vascular ulcers, tunneled/undermined wounds, surgical wounds, (donor sites/grafts, post-Mohs surgery, post laser surgery, podiatric, wound dehiscence), trauma wounds (abrasions, lacerations, second-degree burns, skin tears) and draining wounds. The device is intended for one-time use
More about Integra® Flowable Wound Matrix

CHRONIC WOUNDS

What is a Chronic Wound

A chronic wound is a wound that does not heal in an orderly set of stages and in a predictable amount of time the way most wounds do; wounds that do not heal within three months are often considered chronic.

Chronic wounds may never heal or may take years to do so. These wounds cause patients severe emotional and physical stress and create a significant financial burden on patients and the whole healthcare system.

Acute and chronic wounds are at opposite ends of a spectrum of wound healing types that progress toward being healed at different rates.

COLLAGEN RECONSTRUCTION

INTEGRA DERMAL REGENERATION TEMPLATE DOUBLE LAYER (SKIN)

A two-layer skin regeneration system. The outer layer is made of a thin silicone film that acts as your skin’s epidermis. It protects the wound from infection and controls both heat and moisture loss. The inner layer is constructed of a complex matrix of cross-linked fibres. This porous material acts as a scaffold for regenerating dermal skin cells, which enables the re-growth of a functional dermal layer of skin. Once dermal skin has regenerated, the silicone outer layer is removed and replaced with a thin epidermal skin graft. This completes the procedure and leaves you with flexible, growing skin.

More about Integra® Dermal Regeneration Template Double Layer

INTEGRA DERMAL REGENERATION TEMPLATE SINGLE LAYER (SKIN)

An advanced wound care device comprised of a porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan. The collagen- glycosaminoglycan biodegradable matric provides a scaffold for cellular invasion and capillary growth. It is indicated for the postexcisional treatment of full thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision.

Available in various sizes.

  • IDRT-SL 5cm x 5cm
  • IDRT-SL 10cm x 12,5cm
  • IDRT-SL 10cm x 25cm
  • IDRT-SL 20cm x 25cm

Indications:

INTEGRA® Dermal Regeneration Template is indicated for the postexcisional treatment of full-thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision or not desirable due to the physiological condition of the patient.

INTEGRA® Dermal Regeneration Template is also indicated for use in reconstruction of postexcisional, full-thickness defects of the integument where there is, in the opinion of the treating surgeon, a potential benefit to the patient by improving the reconstructive outcome or decreasing their mortality/morbidity.

More about Integra® Dermal Regeneration Template Single Layer

Integra® Meshed Bilayer Wound Matrix

INTEGRA™ Meshed Bilayer Wound Matrix was specifically designed to be used in conjunction with Negative Pressure Wound Therapy. It is an advanced wound care device comprised of porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan and a semi-permeable polysiloxane (silicone) layer. The meshed bilayer allows drainage of wound exudate and provides a flexible adherent covering for the wound surface. The collagen- glycosaminoglycan biodegradeable matrix provides a scaffold for cellular invasion and capillary growth.

Benefits of INTEGRA™ Meshed Bilayer Wound Matrix include:

  • The consistent meshed design allows better conformity to the wound bed and ease of handling
  • May be used in conjunction with negative pressure wound therapy
  • Allows drainage of wound exudate and provides a flexible, adherent covering for the wound surface
  • Provides immediate wound coverage
  • Highly conformable for various anatomical sites
  • Excellent performance in deep donor sites
  • Room temperature storage
  • Long shelf life
More about Integra® Meshed Double Layer Dermal Regeneration

ReCell®

Activated. Available. Autologous. Complete™

The ReCell® device is used to create a Regenerative Epithelial Suspension – RES™ – which can be used in conjunction with conventional treatments for burns and reconstructive procedures.

ReCell® has been safely used in thousands of procedures worldwide and offers distinct advantages.

  • Definitive Closure with Less Donor Skin
  • Faster epithelialisation of widely-meshed skin graft interstices, decreasing donor skin requirements in mixed depth injuries
  • Smaller donor sites: just 1/80th of the treatment area, for partial thickness injuries like scalds
  • Well suited for large TBSA cases. Can treat up to 1920 cm2

 

Health Economic Benefits:

  • Earlier definitive closure shortens hospital stays
  • Reduced follow-on reconstructive procedures
  • Reduced requirement for scar management
  • Reduced re-admission for closure surgery. Superior Outcomes
  • Regenerated skin has a superior appearance compared with meshed autograft alone.
  • Regenerated skin exhibits more normal collagen formation

 

ReCell®:

  • Activated. Available. Autologous. Complete™
More about Avita Regen

Pressure ulcers

COLLAGEN RECONSTRUCTION

INTEGRA DERMAL REGENERATION TEMPLATE DOUBLE LAYER (SKIN)

A two-layer skin regeneration system. The outer layer is made of a thin silicone film that acts as your skin’s epidermis. It protects the wound from infection and controls both heat and moisture loss. The inner layer is constructed of a complex matrix of cross-linked fibres. This porous material acts as a scaffold for regenerating dermal skin cells, which enables the re-growth of a functional dermal layer of skin. Once dermal skin has regenerated, the silicone outer layer is removed and replaced with a thin epidermal skin graft. This completes the procedure and leaves you with flexible, growing skin.

More about Integra® Dermal Regeneration Template Double Layer

INTEGRA DERMAL REGENERATION TEMPLATE SINGLE LAYER (SKIN)

An advanced wound care device comprised of a porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan. The collagen- glycosaminoglycan biodegradable matric provides a scaffold for cellular invasion and capillary growth. It is indicated for the postexcisional treatment of full thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision.

Available in various sizes.

  • IDRT-SL 5cm x 5cm
  • IDRT-SL 10cm x 12,5cm
  • IDRT-SL 10cm x 25cm
  • IDRT-SL 20cm x 25cm

Indications:

INTEGRA® Dermal Regeneration Template is indicated for the postexcisional treatment of full-thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision or not desirable due to the physiological condition of the patient.

INTEGRA® Dermal Regeneration Template is also indicated for use in reconstruction of postexcisional, full-thickness defects of the integument where there is, in the opinion of the treating surgeon, a potential benefit to the patient by improving the reconstructive outcome or decreasing their mortality/morbidity.

More about Integra® Dermal Regeneration Template Single Layer

Integra® Meshed Bilayer Wound Matrix

INTEGRA™ Meshed Bilayer Wound Matrix was specifically designed to be used in conjunction with Negative Pressure Wound Therapy. It is an advanced wound care device comprised of porous matrix of cross-linked bovine tendon collagen and glycosaminoglycan and a semi-permeable polysiloxane (silicone) layer. The meshed bilayer allows drainage of wound exudate and provides a flexible adherent covering for the wound surface. The collagen- glycosaminoglycan biodegradeable matrix provides a scaffold for cellular invasion and capillary growth.

Benefits of INTEGRA™ Meshed Bilayer Wound Matrix include:

  • The consistent meshed design allows better conformity to the wound bed and ease of handling
  • May be used in conjunction with negative pressure wound therapy
  • Allows drainage of wound exudate and provides a flexible, adherent covering for the wound surface
  • Provides immediate wound coverage
  • Highly conformable for various anatomical sites
  • Excellent performance in deep donor sites
  • Room temperature storage
  • Long shelf life
More about Integra® Meshed Double Layer Dermal Regeneration

Surgical wounds

LICOX – RECONSTRUCTIVE SURGERY

MONITORING OF FLAPS

Licox Recon probes may be used in free-flaps, pedicle tissue transfer grafts, replanted extremities or other tissue loss that are restored by consecutive microsurgical replantation or reconstruction:

  • Plastic and Reconstructive surgery
  • Hand surgery
  • Cranio-Maxillo-Facial Surgery

Licox Recon probes are designed to be introduced directly into soft tissue for determination of the partial pressure of oxygen (ptiO2) and temperature. The oxygen measured by the Licox Recon probes reflects the relative perfusion state of the tissue. The probes also offer a continuous monitoring tool for detecting ischemia in micro-vascular flaps and tissue connection.

ReCell®

Activated. Available. Autologous. Complete™

The ReCell® device is used to create a Regenerative Epithelial Suspension – RES™ – which can be used in conjunction with conventional treatments for burns and reconstructive procedures.

ReCell® has been safely used in thousands of procedures worldwide and offers distinct advantages.

  • Definitive Closure with Less Donor Skin
  • Faster epithelialisation of widely-meshed skin graft interstices, decreasing donor skin requirements in mixed depth injuries
  • Smaller donor sites: just 1/80th of the treatment area, for partial thickness injuries like scalds
  • Well suited for large TBSA cases. Can treat up to 1920 cm2

 

Health Economic Benefits:

  • Earlier definitive closure shortens hospital stays
  • Reduced follow-on reconstructive procedures
  • Reduced requirement for scar management
  • Reduced re-admission for closure surgery. Superior Outcomes
  • Regenerated skin has a superior appearance compared with meshed autograft alone
  • Regenerated skin exhibits more normal collagen formation

 

ReCell®:

  • Activated. Available. Autologous. Complete™
More about Recell