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 00859389005065 CMCV-009-LRG 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 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
Other products with the same Product Code "FTM"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 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
2 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
3 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
4 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
5 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
6 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
7 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
8 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
9 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
10 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
11 04041543311990 PD0808 PD0808 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
12 04041543311983 PD0606 PD0606 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
13 04041543311976 BP0618 BP0618 Bovine Pericardium 6 x 18 cm Tutopatch™ bovine pericardium 6x18 cm TUTOGEN MEDICAL GMBH
14 04041543311969 BP3322 BP3322 Bovine Pericardium 13 x 22 cm Tutomesh™ bovine pericardium 13x22 cm TUTOGEN MEDICAL GMBH
15 04041543311952 BP3016 BP3016 Bovine Pericardium 10 x 16 cm Tutomesh™ bovine pericardium10x16 cm TUTOGEN MEDICAL GMBH
16 04041543311945 BP1420 BP1420 Bovine Pericardium 14 x 20 cm Tutopatch™ bovine pericardium 14x20 cm TUTOGEN MEDICAL GMBH
17 04041543311921 BP1216 BP1216 Bovine Pericardium 12 x 16 cm Tutopatch™ bovine pericardium 12x16 cm TUTOGEN MEDICAL GMBH
18 04041543311914 BP1212 BP1212 Bovine Pericardium 12 x 12 cm Tutopatch™ bovine pericardium 12x12 cm TUTOGEN MEDICAL GMBH
19 04041543311907 BP1016 BP1016 Bovine Pericardium 10 x 16cm Tutopatch™ bovine pericardium 10x16 cm TUTOGEN MEDICAL GMBH
20 04041543311891 BP1013 BP1013 Bovine Pericardium 10 x 12.5 cm Tutopatch™ bovine pericardium10x12.5 cm TUTOGEN MEDICAL GMBH
21 04041543311884 BP0818 BP0818 Bovine Pericardium 8 x 18 cm Tutopatch™ bovine pericardium 8x18 cm TUTOGEN MEDICAL GMBH
22 04041543311877 BP0816 BP0816 Bovine Pericardium 8 x 16 cm Tutopatch™ bovine pericardium 8x16 cm TUTOGEN MEDICAL GMBH
23 04041543311860 BP0814 BP0814 Bovine pericardium 8 x 14 cm Tutopatch™ bovine pericardium 8x14 cm TUTOGEN MEDICAL GMBH
24 04041543311853 BP0811 BP0811 Bovine Pericardium 8 x 11 cm Tutopatch™ bovine pericardium 8x11 cm TUTOGEN MEDICAL GMBH
25 04041543311846 BP0608 BP0608 Bovine pericardium 6 x 8 cm Tutopatch™ bovine pericardium 6x8 cm TUTOGEN MEDICAL GMBH
26 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. Biotronik BioEnvelope AZIYO BIOLOGICS, INC.
27 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. Biotronik BioEnvelope AZIYO BIOLOGICS, INC.
28 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. Biotronik BioEnvelope AZIYO BIOLOGICS, INC.
29 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. Biotronik BioEnvelope AZIYO BIOLOGICS, INC.
30 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. Biotronik BioEnvelope AZIYO BIOLOGICS, INC.
31 03700386922053 EBO101 EBO101 CEMENT RESTRICTOR TORNIER
32 00889024458963 32-5014-56 32-5014-056-00 NA ZIMMER, INC.
33 00889024458956 32-5014-53 32-5014-053-00 NA ZIMMER, INC.
34 00868623000360 XI-S+ XI0404-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
35 00868623000353 XI-S+ XI0203-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
36 00868623000346 XI-S+ XI0710-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
37 00868623000339 XI-S+ XI0808-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
38 00868623000322 XI-S+ XI0508-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
39 00868623000315 XI-S+ XI0615-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
40 00868623000308 XI-S+ XI0606-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
41 00860002305141 XI-S+ XI0909C-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
42 00860002305134 XI-S+ XI1014B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
43 00860002305127 XI-S+ XI1014A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
44 00860002305110 XI-S+ XI1116B-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
45 00860002305103 XI-S+ XI1116A-S+ Colorado Therapeutics Xenograft Implant COLORADO THERAPEUTICS LLC
46 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. CanGaroo Envelope AZIYO BIOLOGICS, INC.
47 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. CanGaroo Envelope AZIYO BIOLOGICS, INC.
48 00859389005065 CMCV-009-LRG 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. CanGaroo Envelope AZIYO BIOLOGICS, INC.
49 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. CanGaroo Envelope AZIYO BIOLOGICS, INC.
50 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. CanGaroo Envelope AZIYO BIOLOGICS, INC.