The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The MICRO Elite Snare is intended for use in the retrieval and manipulation of a
The MICRO Elite Snare is intended for use in the retrieval and manipulation of atraumatic foreign bodies located in the coronary and peripheral cardiovascular system and the extra-cranial neurovascular anatomy.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The VSI Radial Introducer Sheath is intended for use to facilitate the introduct
The VSI Radial Introducer Sheath is intended for use to facilitate the introduction of guidewires, catheters and other accessory medical devices through the skin into a vein or artery and minimize blood loss associated with such introduction.
The MICRO Elite Snare is intended for use in the retrieval and manipulation of a
The MICRO Elite Snare is intended for use in the retrieval and manipulation of atraumatic foreign bodies located in the coronary and peripheral cardiovascular system and the extra-cranial neurovascular anatomy.
The Guardian hemostasis valves are intended to maintain hemostasis during the us
The Guardian hemostasis valves are intended to maintain hemostasis during the use of diagnostic or interventional devices. Guardian hemostasis valves are indicated for maintaining a seal around diagnostic/interventional devices with outside diameters up to 8F (0.105" or 2.67mm) during diagnostic/interventional procedures. The torque device is provided as an aid for steering the guidewire within the vascular anatomy.
The Guardian hemostasis valves are intended to maintain hemostasis during the us
The Guardian hemostasis valves are intended to maintain hemostasis during the use of diagnostic or interventional devices. Guardian hemostasis valves are indicated for maintaining a seal around diagnostic/interventional devices with outside diameters up to 8F (0.105" or 2.67mm) during diagnostic/interventional procedures.
The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of
The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins and varicosities associated with superficial reflux of the great saphenous vein and for the treatment of incompetence and reflux of superficial veins in the lower extremity.
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)