Other products from "STELLEN MEDICAL, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00855638007194 PC The Skin Graft Mesher is a surigical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
2 00855638007187 2:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
3 00855638007170 3:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
4 00855638007163 4:1 The Skin Graft Mesher is surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
5 00855638007156 6:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
6 00855638007149 1:1 The Skin Graft Mesher is a surgical instrument designed to expand skin grafts. FZW Expander, Surgical, Skin Graft 1 Brennen Skin Graft Mesher
7 00855638007101 GPC-0025 GPC-0025 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic U GlucanPro
8 00855638007088 GPC-0085 GPC-0085 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers, venous, diabetic and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic U GlucanPro
9 00855638007064 GPC3-0180 GPC3-0180 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic U GlucanPro 3000
10 00855638007040 GPC3-0035 GPC3-0035 GlucanPro Cream is intended to be used as an aid in the management of superficia GlucanPro Cream is intended to be used as an aid in the management of superficial abrasions, scrapes, cuts and lacerations; minor burns and scalds, partial and full thickness wounds, and irritations of the skin. GlucanPro Cream may also be used, under the supervision/direction of a health care professional for pressure ulcers; venous, diabetic, and arterial ulcers; partial thickness burns; donor graft sites; and surgical wounds.GlucanPro Cream provides a moist environment which supports in the autolytic debridement of wounds with scattered areas of necrosis and slough. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic GlucanPro 3000
11 00855638007125 GEL-6505 GEL-6505 : NovaGel is indicated for use as a scar management dressing on old and new hyp : NovaGel is indicated for use as a scar management dressing on old and new hypertrophic or keloid scars. MDA Elastomer, Silicone, For Scar Management Nova Gel
12 00855638007033 3102-2152 Acellular dermal matrix FTM Mesh, Surgical 2 ProLayer Xenograft
13 00855638007026 3102-2147 Acellular Dermal Matrix FTM Mesh, Surgical 2 ProLayer Xenograft
14 00855638007019 3102-2144 Acellular Dermal Matrix FTM Mesh, Surgical 2 ProLayer Xenograft
15 M070PR05101 PR-0510 PR-0510 Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in proc Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in procedures such as achilles repair, rotator cuff and ligaments. FTM Mesh, Surgical 2 Proformix
16 M070PR04071 PR-0407 PR-04074 Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in proc Multi-purpose implantable surgical mesh, collagen, bioabsorbable-for use in procedures such as achilles repair, rotator cuff and ligaments. FTM Mesh, Surgical 2 Proformix
17 M070PR02051 PR-0205 PR-0205 Multi-purpose Implantable surgical mesh, collagen, bioabsorable- for use in proc Multi-purpose Implantable surgical mesh, collagen, bioabsorable- for use in procedure such as achilles repair, rotator cuff and ligments. FTM Mesh, Surgical 2 Proformix
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.