COPIOS® Pericardium Membrane is a natural collagenous membrane for use in period
COPIOS® Pericardium Membrane is a natural collagenous membrane for use in periodontal and/or dental surgical procedures.
COPIOS® Pericardium Membrane is a natural collagenous membrane for use in period
COPIOS® Pericardium Membrane is a natural collagenous membrane for use in periodontal and/or dental surgical procedures.
COPIOS® Pericardium Membrane is a natural collagenous membrane for use in period
COPIOS® Pericardium Membrane is a natural collagenous membrane for use in periodontal and/or dental surgical procedures.
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine pr
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed,Mesh, surgical,PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE,Mesh, surgical, collagen, plastic and reconstructive surgery
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine
Fortiva™ porcine dermis is an extracellular collagen matrix comprised of porcine dermal tissue that has been processed and terminally sterilized via gamma irradiation. The surgical mesh device is designed to perform as a scaffold that allows for neovascularization and permits replacement of the device with patient’s tissue. The sterile device is supplied pre-hydrated in water and is provided in various sizes. The device is ready for immediate use without extra preparation (i.e., no rinsing, no s
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine pr
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed,Mesh, surgical,PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE,Mesh, surgical, collagen, plastic and reconstructive surgery
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine pr
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed,PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE,Mesh, surgical,Mesh, surgical, collagen, plastic and reconstructive surgery
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine pr
Mesh, surgical, non-synthetic, urogynecologic, for apical vaginal and uterine prolapse, transabdominally placed,PATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE,Mesh, surgical,Mesh, surgical, collagen, plastic and reconstructive surgery
2
Tutopatch™ bovine pericardium 6x8 cm
Other products with the same Product Codes"OXH, PAJ, DXZ, FTM"
CryoPatch SG Pulmonary BranchThe CryoPatch SG Pulmonary Human Cardiac Patch is a
CryoPatch SG Pulmonary BranchThe CryoPatch SG Pulmonary Human Cardiac Patch is a human heart valve aseptically recovered from donated human tissue.
CryoPatch® SG Pulmonary Human Cardiac Branch Patch
CryoPatch SG Pulmonary TrunkThe CryoPatch SG Pulmonary Human Cardiac Patch is a
CryoPatch SG Pulmonary TrunkThe CryoPatch SG Pulmonary Human Cardiac Patch is a human heart valve aseptically recovered from donated human tissue.
CryoPatch SG Pulmonary Hemi-ArteryThe CryoPatch SG Pulmonary Human Cardiac Patch
CryoPatch SG Pulmonary Hemi-ArteryThe CryoPatch SG Pulmonary Human Cardiac Patch is a human heart valve aseptically recovered from donated human tissue.
CryoPatch® SG Pulmonary Human Cardiac Hemi-Artery Patch
VasCure for Vascular Repair is intended for use as a patch material for repair a
VasCure for Vascular Repair is intended for use as a patch material for repair and reconstruction of peripheral vasculature including the carotid, renal, iliac, femoral, and tibial blood vessels. VasCure for Vascular Repair may be used for patch closure of vessels, as a pledget, or for suture line buttressing when repairing peripheral vessels.
VasCure for Vascular Repair is intended for use as a patch material for repair a
VasCure for Vascular Repair is intended for use as a patch material for repair and reconstruction of peripheral vasculature including the carotid, renal, iliac, femoral, and tibial blood vessels. VasCure for Vascular Repair may be used for patch closure of vessels, as a pledget, or for suture line buttressing when repairing peripheral vessels.
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators.
Tyke is intended for use in neonates and infants for repair of pericardial struc
Tyke is intended for use in neonates and infants for repair of pericardial structures, as an epicardial covering for damaged or repaired cardiac structures, as a patch material for intracardiac defects, septal defect and annulus repair, suture-line buttressing, and cardiac repair.
VasCure for Carotid Repair is indicated for use as a patch material for vascular
VasCure for Carotid Repair is indicated for use as a patch material for vascular reconstruction and repair of the carotid artery, including patch closure following carotid endarterectomy and suture-line buttressing.
VasCure for Carotid Repair is indicated for use as a patch material for vascular
VasCure for Carotid Repair is indicated for use as a patch material for vascular reconstruction and repair of the carotid artery, including patch closure following carotid endarterectomy and suture-line buttressing.
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators.
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators.
ProxiCor for Cardiac Tissue Repair is indicated for use as an intracardiac patch
ProxiCor for Cardiac Tissue Repair is indicated for use as an intracardiac patch or pledget for tissue repair and suture-line buttressing.
ProxiCor for Cardiac Tissue Repair is indicated for use as an intracardiac patch
ProxiCor for Cardiac Tissue Repair is indicated for use as an intracardiac patch or pledget for tissue repair and suture-line buttressing.
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators.
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electr
The CanGaroo® Envelope is intended to securely hold a cardiac implantable electronic device or an implantable neurostimulator to create a stable environment when implanted in the body. The cardiac implantable electronic devices that may be used with the CanGaroo® Envelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. The implantable neurostimulator devices that may be used with the CanGaroo® Envelope include vagus nerve stimulators, spinal cordneuromodulators, deep brain stimulators and sacral nerve stimulators.
ProxiCor for Pericardial Closure is a decellularized natural scaffold for repair
ProxiCor for Pericardial Closure is a decellularized natural scaffold for repairing the pericardium following cardiac surgery.
ProxiCor for Pericardial Closure is a decellularized natural scaffold for repair
ProxiCor for Pericardial Closure is a decellularized natural scaffold for repairing the pericardium following cardiac surgery.
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.
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.
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.
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.
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.
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.
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.
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.