PriMatrix® is an acellular dermal tissue matrix derived from fetal bovine dermis
PriMatrix® is an acellular dermal tissue matrix derived from fetal bovine dermis. The device is supplied sterile in a variety of sizes to be trimmed by the surgeon to meet the individual patient’s needs.
PriMatrix® is an acellular dermal tissue matrix derived from fetal bovine dermis
PriMatrix® is an acellular dermal tissue matrix derived from fetal bovine dermis. The device is supplied sterile in a variety of sizes to be trimmed by the surgeon to meet the individual patient’s needs.
PriMatrix® is an acellular dermal tissue matrix derived from fetal bovine dermis
PriMatrix® is an acellular dermal tissue matrix derived from fetal bovine dermis. The device is supplied sterile in a variety of sizes to be trimmed by the surgeon to meet the individual patient’s needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterile a
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterile and is provided in sheet form in a variety of sizes to be trimmed by the surgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterilean
PriMatrix is an acellular dermal tissue matrix. The device is supplied sterileand is provided in sheet form in a variety of sizes to be trimmed by thesurgeon to meet the individual patient's needs.
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fet
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fetal bovine dermis. PriMatrix Ag Antimicrobial is supplied sterile in a variety of sizes that can be trimmed by the surgeon to meet the individual patient's needs. The Ionic Silver content is intended to prevent microbial colonization of the device.
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fet
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fetal bovine dermis. PriMatrix Ag Antimicrobial is supplied sterile in a variety of sizes that can be trimmed by the surgeon to meet the individual patient's needs. The Ionic Silver content is intended to prevent microbial colonization of the device.
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fet
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fetal bovine dermis. PriMatrix Ag Antimicrobial is supplied sterile in a variety of sizes that can be trimmed by the surgeon to meet the individual patient's needs. The Ionic Silver content is intended to prevent microbial colonization of the device.
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fet
PriMatrix Ag Antimicrobial is an acellular dermal tissue matrix derived from fetal bovine dermis. PriMatrix Ag Antimicrobial is supplied sterile in a variety of sizes that can be trimmed by the surgeon to meet the individual patient's needs. The Ionic Silver content is intended to prevent microbial colonization of the device.
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)