No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00840663110384 | ATC1206 | ATC1206 | AlboGraft® Woven with Collagen Bifurcated 12mm x 6mm x 50cm | MAL | Graft, Vascular, Synthetic/Biologic Composite | 2 | AlboGraft Polyester Vascular Graft |
2 | 00840663110377 | ATC6038 | ATC6038 | AlboGraft® Woven with Collagen 38mm x 60cm | MAL | Graft, Vascular, Synthetic/Biologic Composite | 2 | AlboGraft Polyester Vascular Graft |
3 | 00840663110360 | ATC6034 | ATC6034 | AlboGraft® Woven with Collagen 34mm x 60cm | MAL | Graft, Vascular, Synthetic/Biologic Composite | 2 | AlboGraft Polyester Vascular Graft |
4 | 00840663109975 | A4GW6 | A4GW6 | Latis Silicone Graft Cleaning Catheter | DXE | Catheter, Embolectomy | 2 | Latis Silicone Graft Cleaning Catheter |
5 | 00840663109968 | A4G02 | A4G02 | Latis Silicone Graft Cleaning Catheter | DXE | Catheter, Embolectomy | 2 | Latis Silicone Graft Cleaning Catheter |
6 | 00840663109951 | A4G00 | A4G00 | Latis Silicone Graft Cleaning Catheter | DXE | Catheter, Embolectomy | 2 | Latis Silicone Graft Cleaning Catheter |
7 | 00840663109609 | 4001-05 | 4001-05 | Anastoclip Atraumatic Forceps, 20cm | HTD | Forceps | 1 | Anastoclip Atraumatic Forceps |
8 | 00840663109227 | e10P16T | e10P16T | XenoSure Thick Biologic Patch, 10 x 16cm - eP | FTM | Mesh, Surgical | 2 | XenoSure Thick Biologic Patch |
9 | 00840663109210 | e6P8T | e6P8T | XenoSure Thick Biologic Patch, 6 x 8cm - eP | FTM | Mesh, Surgical | 2 | XenoSure Thick Biologic Patch |
10 | 00840663108688 | HJL016-40-N | HJL016-40-N | ProCol Biologic Vascular Graft, 6mm x 40 cm | LXA | Tissue Graft Of 6mm And Greater | 3 | ProCol Biologic Vascular Graft |
11 | 00840663108671 | HJL016-30-N | HJL016-30-N | ProCol Biologic Vascular Graft, 6mm x 30 cm | LXA | Tissue Graft Of 6mm And Greater | 3 | ProCol Biologic Vascular Graft |
12 | 00840663108664 | HJL016-25-N | HJL016-25-N | ProCol Biologic Vascular Graft, 6mm x 25 cm | LXA | Tissue Graft Of 6mm And Greater | 3 | ProCol Biologic Vascular Graft |
13 | 00840663108657 | HJL016-10-N | HJL016-10-N | ProCol Biologic Vascular Graft, 6mm x 10 cm | LXA | Tissue Graft Of 6mm And Greater | 3 | ProCol Biologic Vascular Graft |
14 | 00840663107407 | ATC6007 | ATC6007 | AlboGraft Polyester Vascular Graft 60cmx7mm | MAL | Graft, Vascular, Synthetic/Biologic Composite | 2 | AlboGraft Polyester Vascular Graft |
15 | 00840663107391 | 7210387F | 7210387F | TRIVEX System Resector handpiece, refurbished | DWQ | Stripper, Vein, External | 2 | Trivex System |
16 | 00840663107384 | ATC1536 | ATC1536 | AlboGraft Polyester Vascular Graft 15cmx36mm | MAL | Graft, Vascular, Synthetic/Biologic Composite | 2 | AlboGraft Polyester Vascular Graft |
17 | 00840663107377 | e2400-52 | e2400-52 | Reddick Cholangiogram Catheter with Needle Introducer, eIFU | GBZ | Catheter, Cholangiography | 1 | Reddick Cholangiogram Catheter |
18 | 00840663107285 | 4001-07 | 4001-07 | Anastoclip Atraumatic Forceps, 20cm | HTD | Forceps | 1 | Anastoclip Atraumatic Forceps |
19 | 00840663107278 | 2400-53 | 2400-53 | Reddick Cholangiogram Stiffer Catheter with Needle Introducer | GBZ | Catheter, Cholangiography | 1 | Reddick Cholangiogram Catheter |
20 | 00840663106912 | e2400-53 | e2400-53 | Reddick Cholangiogram Stiffer Catheter with Needle Introducer, eIFU | GBZ | Catheter, Cholangiography | 1 | Reddick Cholangiogram Catheter |
21 | 00840663106905 | 2400-52 | 2400-52 | Reddick Cholangiogram Catheter with Needle Introducer | GBZ | Catheter, Cholangiography | 1 | Reddick Cholangiogram Catheter |
22 | 00840663106899 | 2400-50 | 2400-50 | Reddick Cholangiogram Catheter, 4F | GBZ | Catheter, Cholangiography | 1 | Reddick Cholangiogram Catheter |
23 | 00840663106738 | 7210115 | 7210115 | Trivex System Replacement Lamp | DWQ | Stripper, Vein, External | 2 | Trivex System |
24 | 00840663106677 | ATC3036 | ATC3036 | AlboGraft Polyester Vascular Graft 30cmx36mm | DSY | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter | 2 | AlboGraft Polyester Vascular Graft |
25 | 00840663106646 | 7205683 | 7205683 | Autoclavable Storage and Sterilization Tray (20”x9”x2”) | DWQ | Stripper, Vein, External | 2 | Trivex System |
26 | 00840663106639 | 7209513 | 7209513 | TRIVEX System Illuminator Tubing | DWQ | Stripper, Vein, External | 2 | Trivex System |
27 | 00840663106622 | 7209515 | 7209515 | 5.5mm TRIVEX System Resector Kit (blade and tubing) | DWQ | Stripper, Vein, External | 2 | Trivex System |
28 | 00840663106615 | 7209514 | 7209514 | 4.5mm TRIVEX System Resector Kit (blade and tubing) | DWQ | Stripper, Vein, External | 2 | Trivex System |
29 | 00840663106608 | 2141 | 2141 | VERSITIP, ACMI adaptor for instrument end | DWQ | Stripper, Vein, External | 2 | Trivex System |
30 | 00840663106592 | 7210375 | 7210375 | VERSITIP, TRIVEX adaptor for control unit end | DWQ | Stripper, Vein, External | 2 | Trivex System |
31 | 00840663106585 | 7205180 | 7205180 | GEMINI Universal Light guide, 4mm x 10ft | DWQ | Stripper, Vein, External | 2 | Trivex System |
32 | 00840663106578 | 7210351 | 7210351 | TRIVEX System Illuminator | DWQ | Stripper, Vein, External | 2 | Trivex System |
33 | 00840663106561 | 7210387 | 7210387 | TRIVEX System Resector handpiece | DWQ | Stripper, Vein, External | 2 | Trivex System |
34 | 00840663106554 | 7209791 | 7209791 | TRIVEX System footswitch | DWQ | Stripper, Vein, External | 2 | Trivex System |
35 | 00840663106547 | 7210414 | 7210414 | Trivex System cart | DWQ | Stripper, Vein, External | 2 | Trivex System |
36 | 00840663106530 | 7210386 | 7210386 | Trivex System control unit with build in pump | DWQ | Stripper, Vein, External | 2 | Trivex System |
37 | 00840663106523 | 7210477 | 7210477 | Trivex System | DWQ | Stripper, Vein, External | 2 | Trivex System |
38 | 00840663105908 | 4500-50 | 4500-50 | MultiTASC Dissection/Transection Device sizing tool | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device sizing tool |
39 | 00840663105892 | 4500-10 | 4500-10 | MultiTASC Dissection/Transection Device, 12mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
40 | 00840663105885 | 4500-09 | 4500-09 | MultiTASC Dissection/Transection Device, 11mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
41 | 00840663105878 | 4500-08 | 4500-08 | MultiTASC Dissection/Transection Device, 10mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
42 | 00840663105861 | 4500-07 | 4500-07 | MultiTASC Dissection/Transection Device, 9mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
43 | 00840663105854 | 4500-06 | 4500-06 | MultiTASC Dissection/Transection Device, 8mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
44 | 00840663105847 | 4500-05 | 4500-05 | MultiTASC Dissection/Transection Device, 7mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
45 | 00840663105830 | 4500-04 | 4500-04 | MultiTASC Dissection/Transection Device, 6mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
46 | 00840663105823 | 4500-03 | 4500-03 | MultiTASC Dissection/Transection Device, 5mm | DWX | Stripper, Artery, Intraluminal | 2 | MultiTASC Dissection/Transection Device |
47 | 00840663105519 | T07050 | T07050 | LifeSpan ePTFE Vascular Graft | DSY | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter | 2 | LifeSpan ePTFE Vascular Graft |
48 | 00840663105403 | R10080 | R10080 | LifeSpan ePTFE Vascular Graft | DSY | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter | 2 | LifeSpan ePTFE Vascular Graft |
49 | 00840663105137 | R05010 | R05010 | LifeSpan ePTFE Vascular Graft | DSY | Prosthesis, Vascular Graft, Of 6mm And Greater Diameter | 2 | LifeSpan ePTFE Vascular Graft |
50 | 00840663104536 | ATC6030 | ATC6030 | AlboGraft Polyester Vascular Graft 60cmx30mm | MAL | Graft, Vascular, Synthetic/Biologic Composite | 2 | AlboGraft Polyester Vascular Graft |
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. |