Hydrogel FOXSEAL Vented Dressing - Chest seal dressing for open chest wounds (Sw
Hydrogel FOXSEAL Vented Dressing - Chest seal dressing for open chest wounds (Swedish/ Norwegian/ English CE&US pack)
Hydrogel FOXSEAL Vented Dressing - Chest seal dressing for open chest wounds (Fr
Hydrogel FOXSEAL Vented Dressing - Chest seal dressing for open chest wounds (French/German/ English pack)
Hydrogel FOXSEAL Vented Dressing - Chest seal dressing for open chest wounds (En
Hydrogel FOXSEAL Vented Dressing - Chest seal dressing for open chest wounds (English CE/US pack)
Hemostatic Gauze: The device is indicated for: Temporary external treatment for
Hemostatic Gauze: The device is indicated for: Temporary external treatment for controlling moderate to severe bleeding. Temporary topical dressing for bleeding control associated with minor wounds including control of minor external bleeding and exudate from sutures and/or surgical procedures. Hemostatic gauze is for temporary external use only.
Hemostatic Gauze Pads: The device is indicated for: temporary external use to co
Hemostatic Gauze Pads: The device is indicated for: temporary external use to control moderate to severe bleeding. Hemostatic gauze is for temporary external use only
Hemostatic Gauze Pad. The device is indicated for temporary external use to cont
Hemostatic Gauze Pad. The device is indicated for temporary external use to control moderate to severe bleeding. The hemostatic gauze is for temporary external use only.
Hemostatic Z-Fold Gauze - Non-woven gauze coated with Celox hemostatic granules.
Hemostatic Z-Fold Gauze - Non-woven gauze coated with Celox hemostatic granules. The dressing is indicated for temporary external use to control bleeding of lacerations, minor cuts, and abrasions. For use by trained emergency responders.
Hemostatic Granules in an Applicator - Indicated for Temporary traumatic wound t
Hemostatic Granules in an Applicator - Indicated for Temporary traumatic wound treatment to control moderate to severe bleeding. For temporary external use only
Hemostatic Gauze. The device is indicated for: Temporary external treatment to c
Hemostatic Gauze. The device is indicated for: Temporary external treatment to control moderate to severe bleeding Temporary topical dressing for bleeding control associated with minor wounds including control of minor external bleeding and exudate from sutures and/or surgical procedures.Hemostatic gauze is for temporary external use only
Hemostatic Z-Fold Gauze. Dressing indicated for temporary external use to contro
Hemostatic Z-Fold Gauze. Dressing indicated for temporary external use to control moderate to severe bleeding. For use by trained emergency responders.Chito-R Technology
Haemostatic Gauze Pad: Non-woven gauze coated with Celox haemostatic granules. D
Haemostatic Gauze Pad: Non-woven gauze coated with Celox haemostatic granules. Device is indicated for temporary external use to control bleeding of minor cuts, lacerations, and abrasions.
Hemostatic Gauze: Hemostatic Gauze Pads coated with CELOX granules. Indicated fo
Hemostatic Gauze: Hemostatic Gauze Pads coated with CELOX granules. Indicated for temporary external use to control bleeding of lacerations, minor cuts, and abrasions.
Hemostatic Gauze: Hemostatic gauze dressing coated with Celox Granules. Device i
Hemostatic Gauze: Hemostatic gauze dressing coated with Celox Granules. Device is indicated for temporary external use to control bleeding of lacerations, minor cuts, and abrasions.
Hemostatic Granules: the device is indicated for the local management of bleedin
Hemostatic Granules: the device is indicated for the local management of bleeding such as lacerations, minor cuts and abrasions. The device is for temporary external use only.
Hemostatic Gauze: The device is indicated for temporary external use to control
Hemostatic Gauze: The device is indicated for temporary external use to control bleeding of lacerations, minor cuts and abrasions. Hemostatic gauze is for temporary external use only.
Hemostatic Granules. The device is indicated to control moderate to severe bleed
Hemostatic Granules. The device is indicated to control moderate to severe bleeding. The hemostatic granules are for temporary external use only.
Occlusive dressings for open chest wounds. For use by emergency trained responde
Occlusive dressings for open chest wounds. For use by emergency trained responders (CE& US Swedish/ Norwegian/English Pack)
Haemostatic Gauze: Haemostatic gauze coated with Celox granules. Device is indic
Haemostatic Gauze: Haemostatic gauze coated with Celox granules. Device is indicated to control moderate to severe bleeding. For temporary external use only.
Haemostatic Granules in Applicator. Applicator containing 6g haemostatic granule
Haemostatic Granules in Applicator. Applicator containing 6g haemostatic granules. The device is indicated for temporary traumatic wound treatment to control moderate to severe bleeding.
Hemostatic Granules. For minor external bleeding from wounds and procedures the
Hemostatic Granules. For minor external bleeding from wounds and procedures the device is indicated for use as a temporary topical dressing for bleeding control associated with minor wounds, including control of minor external bleeding and exudate from sutures and/or surgical procedures. For moderate to severe external bleeding wounds the device is indicated for temporary external treatment for controlling moderate to severe bleeding.
Hemostatic Z-Fold Gauze. Dressing indicated for temporary external use to contro
Hemostatic Z-Fold Gauze. Dressing indicated for temporary external use to control moderate to severe bleeding. For use by trained emergency responders.
Haemostatic Gauze: Non-woven Gauze coated with Celox haemostatic granules. Devic
Haemostatic Gauze: Non-woven Gauze coated with Celox haemostatic granules. Device is indicated to control moderate to severe bleeding. For temporary external use only.
Hemostatic Z-fold Gauze Ribbon - Non-woven gauze coated with Celox hemostatic gr
Hemostatic Z-fold Gauze Ribbon - Non-woven gauze coated with Celox hemostatic granules. Dressing is indicated to control moderate to severe bleeding. For emergency temporary external use. Chito-R Technology
Hemostatic Z-fold Gauze. Dressing is indicated to control moderate to severe ble
Hemostatic Z-fold Gauze. Dressing is indicated to control moderate to severe bleeding. For emergency temporary external use. For use by trained emergency responders. Chito-R technology
Hemostatic Z-Fold Gauze - indicated for temporary external use to control bleedi
Hemostatic Z-Fold Gauze - indicated for temporary external use to control bleeding of lacerations, minor cuts and abrasions
Hemostatic Z-Fold Gauze - indicated to control moderate to severe bleeding. For
Hemostatic Z-Fold Gauze - indicated to control moderate to severe bleeding. For emergency temporary external use only.
Hemostatic Pad: The device is indicated for the local management and control of
Hemostatic Pad: The device is indicated for the local management and control of surface bleeding from vascular access sites, percutaneous catheters or tubes utilizing introducer sheaths up to 16 French. The hemostatic pad is for temporary external use only.
Antibacterial Burn Dressing: For the Pre-Hospital Management of 1st and 2nd Degr
Antibacterial Burn Dressing: For the Pre-Hospital Management of 1st and 2nd Degree Burns with Aquanova Ag TechnologyEach dressing contains nominally 0.75% by weight of ionic silver
Antibacterial Burn Wrap - For the Pre-Hospital Management of 1st and 2nd Degree
Antibacterial Burn Wrap - For the Pre-Hospital Management of 1st and 2nd Degree Burns with Aquanova Ag TechnologyEach dressing contains nominally 0.75% by weight of ionic silver
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)