Other products from "NVISION BIOMEDICAL TECHNOLOGIES, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 90814008025315 PLE-015-S PLIF Encoded 10x22 15mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
2 90814008024974 PLE-010-L PLIF Encoded 10x30 10mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
3 90814008024967 PLE-009-L PLIF Encoded 10x30 9mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
4 90814008024950 PLE-008-L PLIF Encoded 10x30 8mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
5 90814008024943 PLE-007-L PLIF Encoded 10x30 7mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
6 90814008024936 PLE-006-L PLIF Encoded 10x30 6mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
7 90814008024929 PLE-615-M PLIF Encoded 10x26 15mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
8 90814008024912 PLE-614-M PLIF Encoded 10x26 14mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
9 90814008024905 PLE-613-M PLIF Encoded 10x26 13mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
10 90814008024899 PLE-612-M PLIF Encoded 10x26 12mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
11 90814008024882 PLE-611-M PLIF Encoded 10x26 11mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
12 90814008024875 PLE-610-M PLIF Encoded 10x26 10mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
13 90814008024868 PLE-609-M PLIF Encoded 10x26 9mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
14 90814008024851 PLE-608-M PLIF Encoded 10x26 8mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
15 90814008024844 PLE-607-M PLIF Encoded 10x26 7mm 6 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
16 90814008024837 PLE-015-M PLIF Encoded 10x26 15mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
17 90814008024820 PLE-014-M PLIF Encoded 10x26 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
18 90814008024813 PLE-013-M PLIF Encoded 10x26 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
19 90814008024806 PLE-012-M PLIF Encoded 10x26 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
20 90814008024790 PLE-011-M PLIF Encoded 10x26 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
21 90814008024783 PLE-010-M PLIF Encoded 10x26 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
22 90814008024776 PLE-009-M PLIF Encoded 10x26 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
23 90814008024769 PLE-008-M PLIF Encoded 10x26 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
24 90814008024752 PLE-007-M PLIF Encoded 10x26 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
25 90814008024745 PLE-006-M PLIF Encoded 10x26 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
26 90814008024738 PLE-014-S PLIF Encoded 10x22 14mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
27 90814008024721 PLE-013-S PLIF Encoded 10x22 13mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
28 90814008024714 PLE-012-S PLIF Encoded 10x22 12mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
29 90814008024707 PLE-011-S PLIF Encoded 10x22 11mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
30 90814008024691 PLE-010-S PLIF Encoded 10x22 10mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
31 90814008024684 PLE-009-S PLIF Encoded 10x22 9mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
32 90814008024677 PLE-008-S PLIF Encoded 10x22 8mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
33 90814008024660 PLE-007-S PLIF Encoded 10x22 7mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
34 90814008024653 PLE-006-S PLIF Encoded 10x22 6mm 0 Degrees MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
35 00810005664905 PD-1000C-750 Caddy 7.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 7.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
36 00810005664899 PD-1000C-650 Caddy 6.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy 6.5 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
37 00810005662253 PD-1000C-475 Caddy 4.75 Screws. The FOCUS Pedicle Screw System is intended for use in the no Caddy 4.75 Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
38 00810005662246 PD-1000C-SS Caddy Set Screws. The FOCUS Pedicle Screw System is intended for use in the non Caddy Set Screws. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
39 00810005662239 PD-1000C-CC Caddy CrossLinks. The FOCUS Pedicle Screw System is intended for use in the non Caddy CrossLinks. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
40 00810005662222 PD-1000C-LR Caddy Lordotic Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Lordotic Rods. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
41 00810005662215 PD-1000C-SR Caddy Straight Rods. The FOCUS Pedicle Screw System is intended for use in the Caddy Straight Rods. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
42 90814008024981 PLE-011-L PLIF Encoded 10x30 11mm 0 Degree MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 nvp
43 00810005662208 PD-1000C-106 Pedicle Screw Case 4 INSERT 4 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 4 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
44 00810005662192 PD-1000C-105 Pedicle Screw Case 4 INSERT 3 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 4 INSERT 3 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
45 00810005662185 PD-1000C-104 Pedicle Screw Case 3 INSERT 2 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 2 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
46 00810005662178 PD-1000C-103 Pedicle Screw Case 3 INSERT 1 Instruments. The FOCUS Pedicle Screw System is in Pedicle Screw Case 3 INSERT 1 Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
47 00810005662161 PD-1000C-102 Pedicle Screw Case, Instruments. The FOCUS Pedicle Screw System is intended for Pedicle Screw Case, Instruments. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
48 00810005662154 PD-1000C-204 Pedicle Screw Case 2 INSERT 3. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 2 INSERT 3. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
49 00810005662147 PD-1000C-211 Pedicle Screw Case 2 Base, Implants. The FOCUS Pedicle Screw System is intended Pedicle Screw Case 2 Base, Implants. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
50 00810005662130 PD-1000C-202 Pedicle Screw Case 1 INSERT 2. The FOCUS Pedicle Screw System is intended for u Pedicle Screw Case 1 INSERT 2. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. LRP Tray, Surgical 1 Focus
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No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00819917022988 209843062 209843062 X-LG 20 DG 11 AND 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
2 00819917022971 209843061 209843061 X-LG 20 DG 9 AND 10 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
3 00819917022964 209843057 209843057 X-LG 15 DG 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
4 00819917022957 209843056 209843056 X-LG 15 DG 10 AND 11 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
5 00819917022940 209843055 209843055 X-LG 15 DG 8 AND 9 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
6 00819917022933 209843054 209843054 X-LG 12 DG 11 AND 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
7 00819917022926 209843053 209843053 X-LG 12 DG 9 AND 10 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
8 00819917022919 209843052 209843052 X-LG 12 DG 7 AND 8 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
9 00819917022902 209843051 209843051 X-LG 10 DG 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
10 00819917022896 209843050 209843050 X-LG 10 DG 10 AND 11 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
11 00819917022889 209843049 209843049 X-LG 10 DG 8 AND 9 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
12 00819917022872 209843048 209843048 X-LG 10 DG 6 AND 7 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
13 00819917022865 209843047 209843047 LG 20 DG 11 AND 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
14 00819917022858 209843046 209843046 LG 20 DG 9 AND 10 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
15 00819917022841 209843042 209843042 LG 15 DG 11 AND 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
16 00819917022834 209843041 209843041 LG 15 DG 9 AND 10 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
17 00819917022827 209843040 209843040 LG 15 DG 7 AND 8 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
18 00819917022810 209843039 209843039 LG 12 DG 11 AND 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
19 00819917022803 209843038 209843038 LG 12 DG 9 AND 10 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
20 00819917022797 209843037 209843037 LG 12 DG 7 AND 8 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
21 00819917022780 209843036 209843036 LG 10 DG 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
22 00819917022773 209843035 209843035 LG 10 DG 10 AND 11 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
23 00819917022766 209843034 209843034 LG 10 DG 8 AND 9 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
24 00819917022759 209843033 209843033 LG 10 DG 6 AND 7 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
25 00819917022742 209843032 209843032 STD 20 DG 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
26 00819917022735 209843031 209843031 STD 20 DG 10 AND 11 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
27 00819917022728 209843030 209843030 STD 20 DG 8 AND 9 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
28 00819917022711 209843026 209843026 STD 15 DG 11 AND 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
29 00819917022704 209843025 209843025 STD 15 DG 9 AND 10 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
30 00819917022698 209843024 209843024 STD 15 DG 7 AND 8 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
31 00819917022681 209843023 209843023 STD 12 DG 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
32 00819917022674 209843022 209843022 STD 12 DG 10 AND 11 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
33 00819917022667 209843021 209843021 STD 12 DG 8 AND 9 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
34 00819917022650 209843016 209843016 STD 12 DG 6 AND 7 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
35 00819917022643 209843020 209843020 STD 10 DG 12 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
36 00819917022636 209843019 209843019 STD 10 DG 10 AND 11 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
37 00819917022629 209843018 209843018 STD 10 DG 8 AND 9 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
38 00819917022612 209843017 209843017 STD 10 DG 6 AND 7 MM H TRL ACIS® ProTi 360™ HL TYBER MEDICAL LLC
39 00819917022605 208843360 208843360 ACIS PROTI 20 DG HL X 12MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
40 00819917022599 208843359 208843359 ACIS PROTI 20 DG HL X 11MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
41 00819917022582 208843358 208843358 ACIS PROTI 20 DG HL X 10MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
42 00819917022575 208843357 208843357 ACIS PROTI 20 DG HL X 9MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
43 00819917022568 208843351 208843351 ACIS PROTI 15 DG HL X 12MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
44 00819917022551 208843350 208843350 ACIS PROTI 15 DG HL X 11MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
45 00819917022544 208843349 208843349 ACIS PROTI 15 DG HL X 10MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
46 00819917022537 208843348 208843348 ACIS PROTI 15 DG HL X 9MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
47 00819917022520 208843347 208843347 ACIS PROTI 15 DG HL X 8MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
48 00819917022513 208843346 208843346 ACIS PROTI 12 DG HL X 12MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
49 00819917022506 208843345 208843345 ACIS PROTI 12DG HL X 11MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC
50 00819917022490 208843344 208843344 ACIS PROTI 12 DG HL X 10MM H ACIS® ProTi 360™ HL TYBER MEDICAL LLC