The Restrata™ Wound Matrix is a sterile, single use device intended for use in l
The Restrata™ Wound Matrix is a sterile, single use device intended for use in local management of wounds. The Restrata™ Wound Matrix is a soft, white, conformable, non-friable, absorbable matrix that acts as a protective covering for wound defects, providing a moist environment for the body’s natural healing process to occur.
The Restrata™ Wound Matrix is a sterile, single use device intended for use in l
The Restrata™ Wound Matrix is a sterile, single use device intended for use in local management of wounds. The Restrata™ Wound Matrix is a soft, white, conformable, non-friable, absorbable matrix that acts as a protective covering for wound defects, providing a moist environment for the body’s natural healing process to occur.
The Restrata™ Wound Matrix is a sterile, single use device intended for use in l
The Restrata™ Wound Matrix is a sterile, single use device intended for use in local management of wounds. The Restrata™ Wound Matrix is a soft, white, conformable, non-friable, absorbable matrix that acts as a protective covering for wound defects, providing a moist environment for the body’s natural healing process to occur.
The Restrata™ Wound Matrix is a sterile, single use device intended for use in l
The Restrata™ Wound Matrix is a sterile, single use device intended for use in local management of wounds. The Restrata™ Wound Matrix is a soft, white, conformable, non-friable, absorbable matrix that acts as a protective covering for wound defects, providing a moist environment for the body’s natural healing process to occur.
CovoraTM is a sterile,single use device intended for use in partial thickness bu
CovoraTM is a sterile,single use device intended for use in partial thickness burns. CovoraTM is a soft, conformable, non-friable, absorbable matrix that provides an environment for the body’s natural healing process to occur
CovoraTM is a sterile,single use device intended for use in partial thickness bu
CovoraTM is a sterile,single use device intended for use in partial thickness burns. CovoraTM is a soft, conformable, non-friable, absorbable matrix that provides an environment for the body’s natural healing process to occur
CovoraTM is a sterile,single use device intended for use in partial thickness bu
CovoraTM is a sterile,single use device intended for use in partial thickness burns. CovoraTM is a soft, conformable, non-friable, absorbable matrix that provides an environment for the body’s natural healing process to occur
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and is to be used with tensionless sutures. Cerafix® Dura Substitute is a soft, white, pliable, nonfriable, porous polymer matrix.
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and is to be used with tensionless sutures. Cerafix® Dura Substitute is a soft, white, pliable, nonfriable, porous polymer matrix.
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and is to be used with tensionless sutures. Cerafix® Dura Substitute is a soft, white, pliable, nonfriable, porous polymer matrix.
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and is to be used with tensionless sutures. Cerafix® Dura Substitute is a soft, white, pliable, nonfriable, porous polymer matrix.
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and is to be used with tensionless sutures. Cerafix® Dura Substitute is a soft, white, pliable, nonfriable, porous polymer matrix.
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and
Cerafix® Dura Substitute is a resorbable implant for repair of dural defects and is to be used with tensionless sutures. Cerafix® Dura Substitute is a soft, white, pliable,nonfriable, porous polymer matrix.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
Restrata(R) is a sterile, single use device intended for use in local management
Restrata(R) is a sterile, single use device intended for use in local management of wounds. Restrata(R) is a soft, white, conformable, non-friable, absorbable matrix that provides an environment for the body’s natural healing process to occur.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
The Restrata Wound Matrix is a sterile, single use device intended for use in lo
The Restrata Wound Matrix is a sterile, single use device intended for use in local management of wounds.
BD ChloraShield™ IV Nexiva™ Dressing with Chlorhexidine Gluconate (CHG) Antimicr
BD ChloraShield™ IV Nexiva™ Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial for BD Nexiva™ Closed Catheter Systems, 3.3 x 2.4 in (83 x 60 mm)
BD ChloraShield™ IV Nexiva™ Dressing with CHG Antimicrobial
BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimic
BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 4.0 x 4.3 in (10 x 11 cm) with notch.
BD ChloraShield™ IV Surround Dressing with CHG Antimicrobial
BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 4
BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 4.0 x 4.3 in (10 x 11 cm)
BD ChloraShield™ IV Dressing with CHG Antimicrobial
BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimic
BD ChloraShield™ IV Surround Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 3.0 x 2.4 in (75 x 60 mm) with slit.
BD ChloraShield™ IV Surround Dressing with CHG Antimicrobial
BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 3
BD ChloraShield™ IV Dressing with Chlorhexidine Gluconate (CHG) Antimicrobial, 3.0 x 2.4 in (75 x 60 mm)
BD ChloraShield™ IV Dressing with CHG Antimicrobial
Reinforced Gelling Fiber +Ag8 x 12 in. DressingPartial to full thickness wounds:
Reinforced Gelling Fiber +Ag8 x 12 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)
Reinforced Gelling Fiber +Ag6 x 6 in. DressingPartial to full thickness wounds:
Reinforced Gelling Fiber +Ag6 x 6 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)
Reinforced Gelling Fiber +Ag4 x 4.75 in. DressingPartial to full thickness wound
Reinforced Gelling Fiber +Ag4 x 4.75 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)
Reinforced Gelling Fiber +Ag2 x 2 in. DressingPartial to full thickness wounds:
Reinforced Gelling Fiber +Ag2 x 2 in. DressingPartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)
Reinforced Gelling Fiber +Ag.75 x 18 in. RopePartial to full thickness wounds: -
Reinforced Gelling Fiber +Ag.75 x 18 in. RopePartial to full thickness wounds: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)Highly absorbent gelling fibersCohesive fiber constructionEffective antimicrobial silverDirections for use: 1. Clean wound area with an appropriate wound cleanser such as Cardinal Health Wound Cleanser or normal saline solution. Dry surrounding skin thoroughly.2. Remove dressing from packaging and if necessary cut dressing to size using sterile scissors.3. Apply dressing over the wound bed leaving a 1/2-inch overlap. If wound is deep, loosely fill wound ensuring that the dressing does not overlap wound margins. Product will expand to fill the empty wound space once in contact with the exudate. Dressing can be pre-moistened with room temperature sterile water or saline solution before application.4. Cover wound and this primary dressing with a non-occlusive secondary dressing to promote a moist wound healing environment.5. All dressings should be monitored frequently. Remove dressing when clinically indicated, such as leakage, excessive bleeding, increased pain, or after a maximum of 7 days. IndicationsMay be used for the management of moderate to heavy exuding, partial to full thickness wounds including: -Pressure ulcers-Leg ulcers-Diabetic ulcers-Post-operative surgical wounds-First- and second-degree burns-Graft and donor sites-Trauma wounds (dermal lesions, trauma injuries or incisions)