No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00887517399779 | 6942044 | CoRoent® XLR, 20x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
2 | 00887517399700 | 6941844 | CoRoent® XLR, 18x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
3 | 00887517399335 | 6941644 | CoRoent® XLR, 16x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
4 | 00887517398765 | 6941444 | CoRoent® XLR, 14x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
5 | 00887517398499 | 6941244 | CoRoent® XLR, 12x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
6 | 00887517398420 | 6941044 | CoRoent® XLR, 10x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
7 | 00887517398055 | 6932088 | CoRoent® XLR, 20x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
8 | 00887517397683 | 6931888 | CoRoent® XLR, 18x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
9 | 00887517397256 | 6931688 | CoRoent® XLR, 16x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
10 | 00887517396822 | 6931488 | CoRoent® XLR, 14x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
11 | 00887517396457 | 6931288 | CoRoent® XLR, 12x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
12 | 00887517395641 | 6922088 | CoRoent® XLR, 20x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
13 | 00887517395634 | 6922044 | CoRoent® XLR, 20x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
14 | 00887517395269 | 6921888 | CoRoent® XLR, 18x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
15 | 00887517395252 | 6921844 | CoRoent® XLR, 18x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
16 | 00887517394880 | 6921688 | CoRoent® XLR, 16x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
17 | 00887517394873 | 6921660 | CoRoent® XL Wide, 16x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
18 | 00887517394866 | 6921655 | CoRoent® XL Wide, 16x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
19 | 00887517394859 | 6921650 | CoRoent® XL Wide, 16x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
20 | 00887517394842 | 6921645 | CoRoent® XL Wide, 16x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
21 | 00887517394835 | 6921644 | CoRoent® XLR, 16x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
22 | 00887517394569 | 6921488 | CoRoent® XLR, 14x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
23 | 00887517394552 | 6921460 | CoRoent® XL Wide, 14x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
24 | 00887517394545 | 6921455 | CoRoent® XL Wide, 14x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
25 | 00887517394538 | 6921450 | CoRoent® XL Wide, 14x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
26 | 00887517394521 | 6921445 | CoRoent® XL Wide, 14x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
27 | 00887517394514 | 6921444 | CoRoent® XLR, 14x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
28 | 00887517394149 | 6921288 | CoRoent® XLR, 12x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
29 | 00887517394132 | 6921260 | CoRoent® XL Wide, 12x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
30 | 00887517394125 | 6921255 | CoRoent® XL Wide, 12x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
31 | 00887517394118 | 6921250 | CoRoent® XL Wide, 12x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
32 | 00887517394101 | 6921245 | CoRoent® XL Wide, 12x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
33 | 00887517393791 | 6921244 | CoRoent® XLR, 12x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
34 | 00887517393722 | 6921088 | CoRoent® XLR, 10x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
35 | 00887517393715 | 6921060 | CoRoent® XL Wide, 10x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
36 | 00887517393708 | 6921055 | CoRoent® XL Wide, 10x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
37 | 00887517393395 | 6921050 | CoRoent® XL Wide, 10x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
38 | 00887517393388 | 6921045 | CoRoent® XL Wide, 10x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
39 | 00887517393371 | 6921044 | CoRoent® XLR, 10x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
40 | 00887517393333 | 6920860 | CoRoent® XL Wide, 8x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
41 | 00887517393326 | 6920855 | CoRoent® XL Wide, 8x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
42 | 00887517393319 | 6920850 | CoRoent® XL Wide, 8x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
43 | 00887517393302 | 6920845 | CoRoent® XL Wide, 8x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
44 | 00887517392961 | 6916860 | CoRoent® XL, 16x18x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
45 | 00887517392954 | 6916855 | CoRoent® XL, 16x18x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
46 | 00887517392947 | 6916850 | CoRoent® XL, 16x18x50mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
47 | 00887517392930 | 6916845 | CoRoent® XL, 16x18x45mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
48 | 00887517392923 | 6916840 | CoRoent® XL, 16x18x40mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
49 | 00887517392916 | 6916260 | CoRoent® XL Wide, 16x22x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
50 | 00887517392909 | 6916255 | CoRoent® XL Wide, 16x22x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | M958BSF251000 | BSF-25100 | BioSphere Flex, Large | BioSphere Flex, Large | SYNERGY BIOMEDICAL, LLC | |
2 | M958BSF250500 | BSF-25050 | BioSphere Flex, Medium | BioSphere Flex, Medium | SYNERGY BIOMEDICAL, LLC | |
3 | M958BSF00150 | Large | BSF-00150 | BioSphere Flex SP | SYNERGY BIOMEDICAL, LLC | |
4 | M958BSF00075 | Medium | BSF-00075 | BioSphere Flex SP | SYNERGY BIOMEDICAL, LLC | |
5 | M958BSF000400 | BSF-00040 | BioSphere Flex SP Extremities, Medium | BioSphere Flex SP Extremities, Medium | SYNERGY BIOMEDICAL, LLC | |
6 | M958BSF000300 | BSF-00030 | BioSphere Flex SP Extremities, Small | BioSphere Flex SP Extremities, Small | SYNERGY BIOMEDICAL, LLC | |
7 | M958BPY1000R | 10cc | BPY-100 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
8 | M958BPY1000 | 10cc | BPY-100 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
9 | M958BPY0500V | 5cc | BPY-050 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
10 | M958BPY0500 | 5cc | BPY-050 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
11 | M958BPY0250X | 2.5cc | BPY-025 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
12 | M958BPY0250 | 2.5cc | BPY-025 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
13 | M958BPY0010R | 1cc | BPY-001 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
14 | M958BPY0010 | 1cc | BPY-001 | BioSphere Putty | SYNERGY BIOMEDICAL, LLC | |
15 | M958BMS050RC0 | Replacement Cannula | BMS-050RC | BioSphere MIS | SYNERGY BIOMEDICAL, LLC | |
16 | M958BMS050KT0 | Kit | BMS-050KT | BioSphere MIS | SYNERGY BIOMEDICAL, LLC | |
17 | M896MAR0FUSE5CC1 | MAR0Fuse5cc | MAR0Fuse Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
18 | M896MAR0FUSE5CC1 | MAR0Fuse5cc | MAR0Fuse Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
19 | M896MAR0FUSE1CC1 | MAR0Fuse1cc | MAR0Fuse Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
20 | M896MAR0FUSE1CC1 | MAR0Fuse1cc | MAR0Fuse Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
21 | M896MAR0FUSE10CC1 | MAR0Fuse10cc | MAR0FUSE Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
22 | M896MAR0FUSE10CC1 | MAR0Fuse10cc | MAR0FUSE Demineralized Bone Matrix Gel | MAR0Fuse | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
23 | M896IQSPPP1100 | Paste Mix Plus | IQSP-PP-110 | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. | |
24 | M896IQSPPP1050 | Paste Mix Plux | IQSP-PP-105 | Synthetic bone graft | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
25 | M896IQSPPP1020 | Paste Mix Plus | IQSP-PP-102 | Synthetic bone graft | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
26 | M896IQSPPP1010 | Paste Mix Plus | IQSP-PP-101 | Synthetic Bone Graft | Inqu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
27 | M896IQSPMX1500 | Matrix | IQSP-MX-150 | lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. | InQu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
28 | M896IQSPMX1250 | Matrix | IQSP-MX-125 | lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. | InQu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
29 | M896IQSPGR1300 | Granules | IQSP-GR-130 | lnQu is a resorbable bone void filler intended to fill bony gaps or voids that a lnQu is a resorbable bone void filler intended to fill bony gaps or voids that are not intrinsic to the stability of the bony structure.InQu is intended for use as a bone graft substitute in the skeletal system (extremities and pelvis). lnQu is indicated for use as a bone graft extender in the spine when combined with bone autograft. These defects may be surgically created or result from traumatic injury to the bone. | InQu | ARTERIOCYTE MEDICAL SYSTEMS, INC. |
30 | 18257200121878 | 711015 | Osteoconductive Scaffold Strip, 15cc | Collage | ORTHOFIX INC. | |
31 | 18257200121861 | 711010 | Osteoconductive Scaffold Strip 10 cc | Collage | ORTHOFIX INC. | |
32 | 18257200115136 | 710015 | Collage Osteoconductive Scaffold Putty 15cc | Collage | ORTHOFIX INC. | |
33 | 18257200115129 | 710010 | Collage Osteoconductive Scaffold Putty 10 cc | Collage | ORTHOFIX INC. | |
34 | 18257200115112 | 710005 | Collage Osteoconductive Scaffold Putty, 5cc | Collage | ORTHOFIX INC. | |
35 | 15060155711499 | 910-010Z | 910-010Z | genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. The kit contains a powder filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set insitu or placed in the bead mould mat provided to form beads for implantation. When injected the mixturesets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex.genex® Bone Graft Substitute is MR safe. | Genex Bone Graft Substitute | BIOCOMPOSITES LTD |
36 | 15060155711482 | 910-005Z | 910-005Z | genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. The kit contains a powder filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set insitu or placed in the bead mould mat provided to form beads for implantation. When injected the mixturesets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex.genex® Bone Graft Substitute is MR safe. | Genex Bone Graft Substitute | BIOCOMPOSITES LTD |
37 | 15060155711475 | 910-003Z | 910-003Z | genex® Bone Graft Substitute is a simple to use synthetic absorbable material de genex® Bone Graft Substitute is a simple to use synthetic absorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. The kit contains a powder filled syringe and mixing solution which, when combined, provides a mouldablecohesive paste which may be implanted into open voids/gaps of the musculoskeletal system to set in situ or placed in the bead mould mat provided to form beads for implantation. When injected the mixture sets to form genex® Bone Graft substitute a hard but absorbable matrix. genex® Bone Graft Substituteis supplied sterile. genex® Bone Graft Substitute , accessories and packaging are not made from natural rubber latex. genex® Bone Graft Substitute is MR safe. | Genex Bone Graft Substitute | BIOCOMPOSITES LTD |
38 | 15060155711451 | 620-003 | 620-003 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
39 | 15060155711420 | 910-010 | 910-010 | Genex® Bone Graft Substitute is a simple to use synthetic resorbable material de Genex® Bone Graft Substitute is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form Genex® Bone Graft Substitute a hard but resorbable matrix. Genex® Bone Graft Substitute is supplied sterile. | Genex® | BIOCOMPOSITES LTD |
40 | 15060155711413 | 910-005 | 910-005 | Genex® Bone Graft Substitute is a simple to use synthetic resorbable material de Genex® Bone Graft Substitute is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form Genex® Bone Graft Substiute, a hard but resorbable matrix. Genex® Bone Graft Substitute is supplied sterile. | Genex® | BIOCOMPOSITES LTD |
41 | 15060155711055 | 640-005 | 640-005 | Stimulan® DS Calcium Sulfate Bone Void Filler is provided sterile for single pat Stimulan® DS Calcium Sulfate Bone Void Filler is provided sterile for single patient use. The kit contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together, the resultant paste is to be injected or digitally packed into open bone/gap to cure insitu. The biodegradable, radiopaque mixture is resorbed in approximately 30-60 days when used in accordance with the device labelling. Stimulan® is manufactured from synthetic implant grade calcium sulfate dihydrate (CaS04, 2H20) that resporbs and is replaced with bone during the healing process. Also as the bone void filler is biodegradable and biocompatible; it may be used at an infected site. | Stimulan® DS | BIOCOMPOSITES LTD |
42 | 15060155711048 | 620-020 | 620-020 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
43 | 15060155711031 | 620-010 | 620-010 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
44 | 15060155711024 | 620-005 | 620-005 | STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cu STIMULAN® Rapid Cure provided sterile for single patient use. STIMULAN® Rapid Cure contains calcium sulfate powder and mixing solution in pre-measured quantities so that when mixed together in a sterile mixing bowl, the resultant paste is to be digitally packed into open bone void/gap to set insitu or placed into the mould provided, the mixture sets to form beads. The biodegradable, radiopaque beads are resorbed in approximately 30 – 60 days when used in accordance with the device labelling. STIMULAN® Rapid Cure is manufactured from synthetic implant grade calcium sulfate dihydrate(CaSO4.2H2O) that resorbs and is replaced with bone during the healing process. Also, as the bone void filler beads are biodegradable and biocompatible, they may be used at an infected site. | Stimulan® Rapid Cure | BIOCOMPOSITES LTD |
45 | 15060155710966 | 980-005 | 980-005 | geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe.When injected the mixture sets to form geneX®; a hard but resorbable matrix. | geneX® ds | BIOCOMPOSITES LTD |
46 | 15060155710959 | 980-002 | 980-002 | geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. One component of the matrix prevents soft tissue in-growth until it is resorbed and replaced by new bony tissue. Another component has been shown to act as a scaffold through which new bone grows. The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe.When injected the mixture sets to form geneX®; a hard but resorbable matrix. | geneX® ds | BIOCOMPOSITES LTD |
47 | 15060155710188 | 920-010 | 920-010 | geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. | geneX® putty | BIOCOMPOSITES LTD |
48 | 15060155710171 | 920-005 | 920-005 | geneX® putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. | geneX® Putty | BIOCOMPOSITES LTD |
49 | 15060155710164 | 920-002 | 920-002 | geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Pu geneX® Putty consists of an inorganic framework of calcium based ions. geneX® Putty has been bioengineered to mimic human bone. It is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible. geneX® Putty is a non-setting putty and is supplied sterile. | geneX® putty | BIOCOMPOSITES LTD |
50 | 15060155710157 | 900-010 | 900-010 | geneX® is a simple to use synthetic resorbable material designed to promote rege geneX® is a simple to use synthetic resorbable material designed to promote regeneration of bone in osseous defects. It degrades into component elements normally found in the body and is highly biocompatible.The kit contains a powder and mixing solution which, when combined, provides a mouldable cohesive paste for introduction into a syringe. When injected the mixture sets to form geneX® a hard but resorbable matrix. geneX® is supplied sterile | geneX® | BIOCOMPOSITES LTD |