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
Other products with the same Product Code "ODP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 07899893207183 941.605 PEEK CERVICAL CAGE 7.5 mm NEOSPACE NEOORTHO PRODUTOS ORTOPÉDICOS S/A.
2 07898624868075 941.604 PEEK CERVICAL CAGE 7.0 mm NEOSPACE NEOORTHO PRODUTOS ORTOPÉDICOS S/A.
3 07898624868068 941.603 PEEK CERVICAL CAGE 6.5 mm NEOSPACE NEOORTHO PRODUTOS ORTOPÉDICOS S/A.
4 07898624868051 941.602 PEEK CERVICAL CAGE 6.0 mm NEOSPACE NEOORTHO PRODUTOS ORTOPÉDICOS S/A.
5 07898624868044 941.601 PEEK CERVICAL CAGE 5.5 mm NEOSPACE NEOORTHO PRODUTOS ORTOPÉDICOS S/A.
6 07898624868037 941.600 PEEK CERVICAL CAGE 5.0 mm NEOSPACE NEOORTHO PRODUTOS ORTOPÉDICOS S/A.
7 07640450863928 TRY-BX 20 01-N TRY-BX 20 01-N CERVICAL DISTRACTOR INSTRUMENT BOX TRYPTIK ® TI SPINEART SA
8 07640450863911 TRY-00 SL 10-N TRY-00 SL 10-N ANATOMIC SMOOTH TRIAL LARGE H10 TRYPTIK ® TI SPINEART SA
9 07640450863904 TRY-00 SL 90-N TRY-00 SL 90-N ANATOMIC SMOOTH TRIAL LARGE H09 TRYPTIK ® TI SPINEART SA
10 07640450863898 TRY-00 SL 80-N TRY-00 SL 80-N ANATOMIC SMOOTH TRIAL LARGE H08 TRYPTIK ® TI SPINEART SA
11 07640450863881 TRY-00 SL 70-N TRY-00 SL 70-N ANATOMIC SMOOTH TRIAL LARGE H07 TRYPTIK ® TI SPINEART SA
12 07640450863874 TRY-00 SL 60-N TRY-00 SL 60-N ANATOMIC SMOOTH TRIAL LARGE H06 TRYPTIK ® TI SPINEART SA
13 07640450863867 TRY-00 SL 50-N TRY-00 SL 50-N ANATOMIC SMOOTH TRIAL LARGE H05 TRYPTIK ® TI SPINEART SA
14 07640450863850 TRY-00 SL 45-N TRY-00 SL 45-N ANATOMIC SMOOTH TRIAL LARGE H4.5 TRYPTIK ® TI SPINEART SA
15 07640450863843 TRY-00 SS 10-N TRY-00 SS 10-N ANATOMIC SMOOTH TRIAL SMALL H10 TRYPTIK ® TI SPINEART SA
16 07640450863836 TRY-00 SS 90-N TRY-00 SS 90-N ANATOMIC SMOOTH TRIAL SMALL H09 TRYPTIK ® TI SPINEART SA
17 07640450863829 TRY-00 SS 80-N TRY-00 SS 80-N ANATOMIC SMOOTH TRIAL SMALL H08 TRYPTIK ® TI SPINEART SA
18 07640450863812 TRY-00 SS 70-N TRY-00 SS 70-N ANATOMIC SMOOTH TRIAL SMALL H07 TRYPTIK ® TI SPINEART SA
19 07640450863805 TRY-00 SS 60-N TRY-00 SS 60-N ANATOMIC SMOOTH TRIAL SMALL H06 TRYPTIK ® TI SPINEART SA
20 07640450863799 TRY-00 SS 50-N TRY-00 SS 50-N ANATOMIC SMOOTH TRIAL SMALL H05 TRYPTIK ® TI SPINEART SA
21 07640450863782 TRY-00 SS 45-N TRY-00 SS 45-N ANATOMIC SMOOTH TRIAL SMALL H4.5 TRYPTIK ® TI SPINEART SA
22 07640450863775 TRY-07 SL 10-N TRY-07 SL 10-N LORDOTIC SMOOTH TRIAL LARGE H10 TRYPTIK ® TI SPINEART SA
23 07640450863768 TRY-07 SL 90-N TRY-07 SL 90-N LORDOTIC SMOOTH TRIAL LARGE H09 TRYPTIK ® TI SPINEART SA
24 07640450863751 TRY-07 SL 80-N TRY-07 SL 80-N LORDOTIC SMOOTH TRIAL LARGE H08 TRYPTIK ® TI SPINEART SA
25 07640450863744 TRY-07 SL 70-N TRY-07 SL 70-N LORDOTIC SMOOTH TRIAL LARGE H07 TRYPTIK ® TI SPINEART SA
26 07640450863737 TRY-07 SL 60-N TRY-07 SL 60-N LORDOTIC SMOOTH TRIAL LARGE H06 TRYPTIK ® TI SPINEART SA
27 07640450863720 TRY-07 SL 50-N TRY-07 SL 50-N LORDOTIC SMOOTH TRIAL LARGE H05 TRYPTIK ® TI SPINEART SA
28 07640450863713 TRY-07 SL 45-N TRY-07 SL 45-N LORDOTIC SMOOTH TRIAL LARGE H4.5 TRYPTIK ® TI SPINEART SA
29 07640450863706 TRY-07 SS 10-N TRY-07 SS 10-N LORDOTIC SMOOTH TRIAL SMALL H10 TRYPTIK ® TI SPINEART SA
30 07640450863690 TRY-07 SS 90-N TRY-07 SS 90-N LORDOTIC SMOOTH TRIAL SMALL H09 TRYPTIK ® TI SPINEART SA
31 07640450863683 TRY-07 SS 80-N TRY-07 SS 80-N LORDOTIC SMOOTH TRIAL SMALL H08 TRYPTIK ® TI SPINEART SA
32 07640450863676 TRY-07 SS 70-N TRY-07 SS 70-N LORDOTIC SMOOTH TRIAL SMALL H07 TRYPTIK ® TI SPINEART SA
33 07640450863669 TRY-07 SS 60-N TRY-07 SS 60-N LORDOTIC SMOOTH TRIAL SMALL H06 TRYPTIK ® TI SPINEART SA
34 07640450863652 TRY-07 SS 50-N TRY-07 SS 50-N LORDOTIC SMOOTH TRIAL SMALL H05 TRYPTIK ® TI SPINEART SA
35 07640450863645 TRY-07 SS 45-N TRY-07 SS 45-N LORDOTIC SMOOTH TRIAL SMALL H4.5 TRYPTIK ® TI SPINEART SA
36 07640450863638 TRY-00 RL 10-N TRY-00 RL 10-N ANATOMIC RASP TRIAL LARGE H10 TRYPTIK ® TI SPINEART SA
37 07640450863621 TRY-00 RL 90-N TRY-00 RL 90-N ANATOMIC RASP TRIAL LARGE H09 TRYPTIK ® TI SPINEART SA
38 07640450863614 TRY-00 RL 80-N TRY-00 RL 80-N ANATOMIC RASP TRIAL LARGE H08 TRYPTIK ® TI SPINEART SA
39 07640450863607 TRY-00 RL 70-N TRY-00 RL 70-N ANATOMIC RASP TRIAL LARGE H07 TRYPTIK ® TI SPINEART SA
40 07640450863591 TRY-00 RL 60-N TRY-00 RL 60-N ANATOMIC RASP TRIAL LARGE H06 TRYPTIK ® TI SPINEART SA
41 07640450863584 TRY-00 RL 50-N TRY-00 RL 50-N ANATOMIC RASP TRIAL LARGE H05 TRYPTIK ® TI SPINEART SA
42 07640450863577 TRY-00 RL 45-N TRY-00 RL 45-N ANATOMIC RASP TRIAL LARGE H4.5 TRYPTIK ® TI SPINEART SA
43 07640450863560 TRY-00 RS 10-N TRY-00 RS 10-N ANATOMIC RASP TRIAL SMALL H10 TRYPTIK ® TI SPINEART SA
44 07640450863553 TRY-00 RS 90-N TRY-00 RS 90-N ANATOMIC RASP TRIAL SMALL H09 TRYPTIK ® TI SPINEART SA
45 07640450863546 TRY-00 RS 80-N TRY-00 RS 80-N ANATOMIC RASP TRIAL SMALL H08 TRYPTIK ® TI SPINEART SA
46 07640450863539 TRY-00 RS 70-N TRY-00 RS 70-N ANATOMIC RASP TRIAL SMALL H07 TRYPTIK ® TI SPINEART SA
47 07640450863522 TRY-00 RS 60-N TRY-00 RS 60-N ANATOMIC RASP TRIAL SMALL H06 TRYPTIK ® TI SPINEART SA
48 07640450863515 TRY-00 RS 50-N TRY-00 RS 50-N ANATOMIC RASP TRIAL SMALL H05 TRYPTIK ® TI SPINEART SA
49 07640450863508 TRY-00 RS 45-N TRY-00 RS 45-N ANATOMIC RASP TRIAL SMALL H4.5 TRYPTIK ® TI SPINEART SA
50 07640450863485 TRY-IN 54 00-N TRY-IN 54 00-N EXTRACTION MALLET TRYPTIK ® TI SPINEART SA