Other products from "AZIYO BIOLOGICS, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00859389005102 CMCV-098-204 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 Tyke, Patch, Pledget and Intracardiac
2 00859389005010 CMCV-060-402 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 ProxiCor for Pericardial Closure
3 00859389005003 CMCV-059-401 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene ProxiCor for Pericardial Closure
4 00859389005140 CMCV-013-609 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 VasCure for Vascular Repair
5 00859389005126 CMCV-011-606 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 VasCure for Vascular Repair
6 00859389005096 CMCV-073-609 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 VasCure for Carotid Repair
7 00859389005089 CMCV-072-606 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 VasCure for Carotid Repair
8 00859389005058 CMCV-067-404 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 ProxiCor for Cardiac Tissue Repair
9 00859389005041 CMCV-064-401 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. DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene 2 ProxiCor for Cardiac Tissue Repair
10 04035479160555 440579 The BioEnvelope is intended to securely hold a cardiac implantable electronic de The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. FTM Mesh, Surgical 2 Biotronik BioEnvelope
11 04035479160548 440578 The BioEnvelope is intended to securely hold a cardiac implantable electronic de The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. FTM Mesh, Surgical Biotronik BioEnvelope
12 04035479160531 440577 The BioEnvelope is intended to securely hold a cardiac implantable electronic de The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. FTM Mesh, Surgical Biotronik BioEnvelope
13 04035479160524 440576 The BioEnvelope is intended to securely hold a cardiac implantable electronic de The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. FTM Mesh, Surgical Biotronik BioEnvelope
14 04035479160517 440575 The BioEnvelope is intended to securely hold a cardiac implantable electronic de The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices. FTM Mesh, Surgical Biotronik BioEnvelope
15 00859389005119 CMCV-009-XXL 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. FTM Mesh, Surgical 2 CanGaroo Envelope
16 00859389005072 CMCV-009-XLG 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. FTM Mesh, Surgical 2 CanGaroo Envelope
17 00859389005034 CMCV-009-MED 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. FTM Mesh, Surgical 2 CanGaroo Envelope
18 00859389005027 CMCV-009-SML 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. FTM Mesh, Surgical 2 CanGaroo Envelope
Other products with the same Product Code "FTM"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 07613252204442 81050 81050 MEDPOR TITAN FAN- MTB MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
2 07613252204435 81049 81049 MEDPOR TITAN FAN- MTM MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
3 07613252084792 82020 82020 Cranial Curve - BARRIER MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
4 07613252084785 82019 82019 Cranial Curve MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
5 07613252084815 82030 82030 Posterior Implant MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
6 07613252084402 81040 81040 MEDPOR TITAN MAX Sheet MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
7 07613252084396 81038 81038 Cranial Temporal with Template ? Right MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
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10 07613252084365 81035 81035 MAX Orbital Floor and Wall MTB Left MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
11 07613252084358 81034 81034 MAX Orbital Floor and Wall MTM MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
12 07613252084341 81033 81033 Orbital Floor and Wall BTB MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
13 07613252084334 81032 81032 Orbital Floor and Wall MTB Right MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
14 07613252084327 81031 81031 Orbital Floor and Wall MTB Left MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
15 07613252084310 81030 81030 Orbital Floor and Wall MTM MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
16 07613252084303 81029 81029 MEDPOR TITAN BARRIER (MTB) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
17 07613252084297 81028 81028 MEDPOR TITAN BARRIER (MTB) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
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19 07613252084273 81026 81026 MEDPOR TITAN BARRIER (MTB) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
20 07613252084266 81025 81025 MEDPOR TITAN Double BARRIER (BTB) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
21 07613252084259 81024 81024 MEDPOR TITAN Double BARRIER (BTB) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
22 07613252084242 81023 81023 MEDPOR TITAN MEDPOR (MTM) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
23 07613252084235 81022 81022 MEDPOR TITAN MEDPOR (MTM) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
24 07613252084228 81021 81021 MEDPOR TITAN MEDPOR (MTM) MEDPOR TITAN STRYKER LEIBINGER GMBH & CO. KG
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31 05060260020106 254015XD 254015XD Reconstructive Tissue Matrix SurgiPure® XD TISSUE REGENIX WOUND CARE INC.
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35 05060260020069 152515XD 152515XD Reconstructive Tissue Matrix SurgiPure® XD TISSUE REGENIX WOUND CARE INC.
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41 04041543312096 PD3535 PD3535 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 TUTOGEN MEDICAL GMBH
42 04041543312089 PD3030 PD3030 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 TUTOGEN MEDICAL GMBH
43 04041543312072 PD2035 PD2035 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 TUTOGEN MEDICAL GMBH
44 04041543312065 PD2025 PD2025 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 TUTOGEN MEDICAL GMBH
45 04041543312058 PD2020 PD2020 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 TUTOGEN MEDICAL GMBH
46 04041543312041 PD1620 PD1620 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 TUTOGEN MEDICAL GMBH
47 04041543312034 PD1025 PD1025 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 TUTOGEN MEDICAL GMBH
48 04041543312027 PD1016 PD1016 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 TUTOGEN MEDICAL GMBH
49 04041543312010 PD1010 PD1010 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 TUTOGEN MEDICAL GMBH
50 04041543312003 PD0822 PD0822 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 TUTOGEN MEDICAL GMBH