| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00856072005289 | R20252-1020G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 2 | 00856072005197 | R20253-1122G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 3 | 00856072005142 | R20243-1122P | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 4 | 00856072005111 | R20153-2020G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 5 | 00856072005104 | R20153-1620G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 6 | 00856072005074 | R20143-2020P | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 7 | 00856072005043 | R20143-0416P | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 8 | 00856072005036 | R20252-1122G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 9 | 00856072005029 | R20252-0815G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 10 | 00856072005012 | R20152-2020G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 11 | 00856072005005 | R20152-1620G | OviTex® PRS is for implantation to reinforce soft tissue where weakness exists i OviTex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use. | FTM,FTL | Mesh, Surgical,Mesh, Surgical, Polymeric | 2 | OviTex® PRS | |
| 12 | 00856072005562 | F10333-0822T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 13 | 00856072005555 | F10331-1012T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 14 | 10856072005088 | F10069-1822 | F10069-1822 | TELAMax 1S is a sterile bioscaffold composed of ovine (sheep) derived extracellu TELAMax 1S is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene. The device consists of two sides: a textured and smooth side. The textured side of the device, indicated with blue polypropylene, provides a surface conducive for tissue ingrowth. The smooth side of the device, containing clear polypropylene, provides a surface designed to minimize tissue attachment. TELAMax 1S will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. TELAMax 1S is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient's requirements. | FTM | Mesh, Surgical | 2 | TELAMax 1S |
| 15 | 00856072005654 | F10345-0610T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 16 | 00856072005647 | F10345-0608T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 17 | 00856072005630 | F10340-0608T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 18 | 00856072005623 | F10339-1012T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 19 | 00856072005616 | F10338-0610T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 20 | 00856072005586 | F10335-1012T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 21 | 00856072005579 | F10334-0822T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 22 | 00856072005548 | F10330-0610T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 23 | 00856072005531 | F10329-0610T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 24 | 00856072005272 | F10269-1015T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 25 | 00810055070923 | F10342-1017T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 26 | 00810055070916 | F10341-1016T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | FZX | Guide, Surgical, Instrument | 1 | OviTex® | |
| 27 | 10856072005132 | F10068-0408 | F10068-0408 | TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene. TELAMax will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. TELAMax is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient's requirements. | FTM | Mesh, Surgical | 2 | TELAMax |
| 28 | 10856072005026 | F10068-1010 | F10068-1010 | TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular TELAMax is a sterile bioscaffold composed of ovine (sheep) derived extracellular matrix (ECM) and monofilament polypropylene. TELAMax will incorporate into the recipient tissue with associated cellular and microvascular ingrowth. TELAMax is provided in various shapes and sizes to suit surgeon preference and the complexity of the soft tissue repair. The device may be trimmed to a desired shape to further accommodate an individual patient's requirements. | FTM | Mesh, Surgical | 2 | TELAMax |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 04042301144331 | 6000738 | Ti-Mesh 1.4" X 4" Strong 65g/m² | TiMESH | PFM MEDICAL TITANIUM GMBH | |
| 2 | 04042301144317 | 6000737 | Ti-Mesh 1.4" X 4" Light 35g/m² | TiMESH | PFM MEDICAL TITANIUM GMBH | |
| 3 | 04042301117809 | 6000424 | Ti-MESH 12" X 12" Strong 65g/m² | Ti-MESH | PFM MEDICAL TITANIUM GMBH | |
| 4 | 04042301117786 | 6000423 | Ti-MESH 6' X 8" Strong 65g/m² | Ti-MESH | PFM MEDICAL TITANIUM GMBH | |
| 5 | 04042301117397 | 6000471 | Ti-MESH 6" X 6"Strong 65g/m² | Ti-MESH | PFM MEDICAL TITANIUM GMBH | |
| 6 | 04042301102768 | 6000470 | Ti-MESH 4" X 6" Strong 65g/m² | Ti-MESH | PFM MEDICAL TITANIUM GMBH | |
| 7 | 04042301097668 | 6000139 | Ti-Mesh 12" X 12" Light 35g/m² | TiMESH | PFM MEDICAL TITANIUM GMBH | |
| 8 | 04042301097644 | 6000140 | Ti-Mesh 6" X 8" Light 35g/m² | TiMESH | PFM MEDICAL TITANIUM GMBH | |
| 9 | 04042301097620 | 6000248 | Ti-MESH 6" X 8" Extralight 16g/m² | Ti-MESH | PFM MEDICAL TITANIUM GMBH | |
| 10 | 04042301097606 | 6000312 | Ti-Mesh 6" X 6" Light 35g/m² | TiMESH | PFM MEDICAL TITANIUM GMBH | |
| 11 | 04042301097583 | 6000311 | Ti-MESH 6"x 6" Extralight 16g/m² | Ti-MESH | PFM MEDICAL TITANIUM GMBH | |
| 12 | 04042301097569 | 6000138 | Ti-Mesh 4" X 6" Light 35 g/m² | TiMESH | PFM MEDICAL TITANIUM GMBH | |
| 13 | 04042301097545 | 6000137 | Ti-Mesh 4" X 6" Extra Light 16 g/m² | TiMESH | PFM MEDICAL TITANIUM GMBH | |
| 14 | 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 |
| 15 | 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 |
| 16 | 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 |
| 17 | 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 |
| 18 | 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 |
| 19 | 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 |
| 20 | 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 |
| 21 | 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 |
| 22 | 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 |
| 23 | 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 |
| 24 | 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 |
| 25 | 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 |
| 26 | 04041543311976 | BP0618 | BP0618 | Bovine Pericardium 6 x 18 cm | Tutopatch™ bovine pericardium 6x18 cm | TUTOGEN MEDICAL GMBH |
| 27 | 04041543311969 | BP3322 | BP3322 | Bovine Pericardium 13 x 22 cm | Tutomesh™ bovine pericardium 13x22 cm | TUTOGEN MEDICAL GMBH |
| 28 | 04041543311952 | BP3016 | BP3016 | Bovine Pericardium 10 x 16 cm | Tutomesh™ bovine pericardium10x16 cm | TUTOGEN MEDICAL GMBH |
| 29 | 04041543311945 | BP1420 | BP1420 | Bovine Pericardium 14 x 20 cm | Tutopatch™ bovine pericardium 14x20 cm | TUTOGEN MEDICAL GMBH |
| 30 | 04041543311921 | BP1216 | BP1216 | Bovine Pericardium 12 x 16 cm | Tutopatch™ bovine pericardium 12x16 cm | TUTOGEN MEDICAL GMBH |
| 31 | 04041543311914 | BP1212 | BP1212 | Bovine Pericardium 12 x 12 cm | Tutopatch™ bovine pericardium 12x12 cm | TUTOGEN MEDICAL GMBH |
| 32 | 04041543311907 | BP1016 | BP1016 | Bovine Pericardium 10 x 16cm | Tutopatch™ bovine pericardium 10x16 cm | TUTOGEN MEDICAL GMBH |
| 33 | 04041543311891 | BP1013 | BP1013 | Bovine Pericardium 10 x 12.5 cm | Tutopatch™ bovine pericardium10x12.5 cm | TUTOGEN MEDICAL GMBH |
| 34 | 04041543311884 | BP0818 | BP0818 | Bovine Pericardium 8 x 18 cm | Tutopatch™ bovine pericardium 8x18 cm | TUTOGEN MEDICAL GMBH |
| 35 | 04041543311877 | BP0816 | BP0816 | Bovine Pericardium 8 x 16 cm | Tutopatch™ bovine pericardium 8x16 cm | TUTOGEN MEDICAL GMBH |
| 36 | 04041543311860 | BP0814 | BP0814 | Bovine pericardium 8 x 14 cm | Tutopatch™ bovine pericardium 8x14 cm | TUTOGEN MEDICAL GMBH |
| 37 | 04041543311853 | BP0811 | BP0811 | Bovine Pericardium 8 x 11 cm | Tutopatch™ bovine pericardium 8x11 cm | TUTOGEN MEDICAL GMBH |
| 38 | 04041543311846 | BP0608 | BP0608 | Bovine pericardium 6 x 8 cm | Tutopatch™ bovine pericardium 6x8 cm | TUTOGEN MEDICAL GMBH |
| 39 | 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. | |
| 40 | 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. | |
| 41 | 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. | |
| 42 | 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. | |
| 43 | 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. | |
| 44 | 03760185570381 | CABS06P1 | The BIOMESH® CA.B.S.'Air® prosthesis consists of (according to the references on The BIOMESH® CA.B.S.'Air® prosthesis consists of (according to the references on the box): - A parietal prosthesis made of a plug and a polypropylene mesh and two polyethylene terephthalate and ePTFE fixation threads crimped of stainless steel needles. - A balloon which allows the deployment of the parietal prosthesis | BIOMESH®CA.B.S.'Air® | COUSIN BIOTECH | |
| 45 | 03760193182132 | MSH 13 D16 V | CVM16RUS | Polyester mesh coated with collagen membrane | COVAMESH | BIOM' UP |
| 46 | 03760193182125 | MSH 12 3020 V | CVM3020US | Polyester mesh coated with collagen membrane | COVAMESH | BIOM' UP |
| 47 | 03760193182118 | MSH 11 2520 V | CVM2520US | Polyester mesh coated with collagen membrane | COVAMESH | BIOM' UP |
| 48 | 03760193182101 | MSH 10 2015 V | CVM2015US | Polyester mesh coated with collagen membrane | COVAMESH | BIOM' UP |
| 49 | 03760193182095 | MSH 09 1510 V | CVM1510US | Polyester mesh coated with collagen membrane | COVAMESH | BIOM' UP |
| 50 | 03760193182088 | MSH 08 D12 V | CVM12RUS | Polyester mesh coated with collagen membrane | COVAMESH | BIOM' UP |