Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine f
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment and contains approximately 12 µg/cm² (~0.3% w/w) ionic silver, intended to inhibit colonization of the device.
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine f
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment and contains approximately 12 µg/cm² (~0.3% w/w) ionic silver, intended to inhibit colonization of the device.
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine f
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment and contains approximately 12 µg/cm² (~0.3% w/w) ionic silver, intended to inhibit colonization of the device.
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine f
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment and contains approximately 12 µg/cm² (~0.3% w/w) ionic silver, intended to inhibit colonization of the device.
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine f
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment and contains approximately 12 µg/cm² (~0.3% w/w) ionic silver, intended to inhibit colonization of the device.
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine f
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment and contains approximately 12 µg/cm² (~0.3% w/w) ionic silver, intended to inhibit colonization of the device.
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine f
Endoform™ Antimicrobial Restorative Bioscaffold is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment and contains approximately 12 µg/cm² (~0.3% w/w) ionic silver, intended to inhibit colonization of the device.
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bi
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomac
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment.
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomac
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment.
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomac
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment.
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bi
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bi
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bi
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bi
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bi
OviTex™ Reinforced Tissue Matrix with Permanent Polymer (OviTex) is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene colored with ([phathalocyaninato(2-)] copper). OviTex will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. OviTex is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient’s requirements.
Endoform Surface is intended for applications in plastic and reconstructive surg
Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.
Endoform Surface is intended for applications in plastic and reconstructive surg
Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.
Endoform Surface is intended for applications in plastic and reconstructive surg
Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.
Endoform Surface is intended for applications in plastic and reconstructive surg
Endoform Surface is intended for applications in plastic and reconstructive surgery or to cover, protect, and provide a moist wound environment. The device may be fixed, via sutures, staples, or tacks to the surrounding tissue, if desired.
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomac
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment.
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomac
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment.
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomac
Endoform Antimicrobial Dermal Template is a sterile, single use ovine forestomach-derived extracellular matrix intended to cover, protect, and provide a moist wound environment.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Matrix is intended for applications in plastic and reconstructive surgery
Myriad Matrix is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad is intended for applications in plastic and reconstructive surgery or to
Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad is intended for applications in plastic and reconstructive surgery or to
Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad is intended for applications in plastic and reconstructive surgery or to
Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad is intended for applications in plastic and reconstructive surgery or to
Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad is intended for applications in plastic and reconstructive surgery or to
Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad is intended for applications in plastic and reconstructive surgery or to
Myriad is intended for applications in plastic and reconstructive surgery or to cover, protect and provide a moist wound environment. The device may be fixed, via sutures, staples or tacks to surround the tissue if desired.
Myriad Morcells™ is derived from an extracellular matrix primarily composed of o
Myriad Morcells™ is derived from an extracellular matrix primarily composed of ovine collagen and is supplied as a sterile particulate.
Myriad Morcells™ is derived from an extracellular matrix primarily composed of o
Myriad Morcells™ is derived from an extracellular matrix primarily composed of ovine collagen and is supplied as a sterile particulate.
Symphony™ is a sterile, single use wound dressing manufactured by incorporating
Symphony™ is a sterile, single use wound dressing manufactured by incorporating a layer of glycosaminoglycans between sheets of ovine forestomach-derived extracellular matrix.
Symphony™ is a sterile, single use wound dressing manufactured by incorporating
Symphony™ is a sterile, single use wound dressing manufactured by incorporating a layer of glycosaminoglycans between sheets of ovine forestomach-derived extracellular matrix.
Symphony™ is a sterile, single use wound dressing manufactured by incorporating
Symphony™ is a sterile, single use wound dressing manufactured by incorporating a layer of glycosaminoglycans between sheets of ovine forestomach-derived extracellular matrix.
Ovitex® PRS is for implantation to reinforce soft tissue where weakness exists i
Ovitex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use.
NuMed Silver Alginate Rope Dressing, conformable wound dressings with a high man
NuMed Silver Alginate Rope Dressing, conformable wound dressings with a high mannuronic acid content. The silver impregnated alginate fibers, 1.4% w/w silver as silver calcium alginate per dressing, forms a gel when in contact with wound exudate or blood, which creates a moist wound healing environment. The silver in the alginate wound dressing has an antibacterial effect on various types of bacteria including; Staphylococcus aureus and E coli. The sustained release of silver ions protects the dressing from a broad spectrum of bacterial contamination over a period of up to 3 days.
NuMed Silver Alginate 4x5 Dressing, conformable wound dressings with a high mann
NuMed Silver Alginate 4x5 Dressing, conformable wound dressings with a high mannuronic acid content. The silver impregnated alginate fibers, 1.4% w/w silver as silver calcium alginate per dressing, forms a gel when in contact with wound exudate or blood, which creates a moist wound healing environment. The silver in the alginate wound dressing has an antibacterial effect on various types of bacteria including; Staphylococcus aureus and E coli. The sustained release of silver ions protects the dressing from a broad spectrum of bacterial contamination over a period of up to 3 days.
NuMed Silver Alginate 2x2 Dressing, conformable wound dressings with a high mann
NuMed Silver Alginate 2x2 Dressing, conformable wound dressings with a high mannuronic acid content. The silver impregnated alginate fibers, 1.4% w/w silver as silver calcium alginate per dressing, forms a gel when in contact with wound exudate or blood, which creates a moist wound healing environment. The silver in the alginate wound dressing has an antibacterial effect on various types of bacteria including; Staphylococcus aureus and E coli. The sustained release of silver ions protects the dressing from a broad spectrum of bacterial contamination over a period of up to 3 days.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic
BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms.
Saljet 6 is a single use disposable polymer vial with a twist off top containing
Saljet 6 is a single use disposable polymer vial with a twist off top containing 30ml of sterile normal saline 0.9% w/v. It contains no preservatives, surfactants or buffering. The vials are packed into an outer shelf carton. six vials per carton.
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 Z-Fold Gauze - Non-woven gauze coated with Celox hemostatic granules
Hemostatic Z-Fold Gauze - Non-woven gauze coated with Celox hemostatic granules with Chito-R technology. Dressing is indicated for temporary external use to control bleeding of lacerations, minor cuts, and abrasions. For use by a trained emergency responder.
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 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 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
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 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.
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.