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 "HTR"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00814008023226 AC-1416T-415 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
2 00814008023219 AC-1416T-414 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
3 00814008023202 AC-1416T-413 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
4 00814008023196 AC-1416T-412 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
5 00814008023189 AC-1416T-411 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
6 00814008023172 AC-1416T-410 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
7 00814008023165 AC-1416T-409 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
8 00814008023158 AC-1416T-408 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
9 00814008023141 AC-1416T-407 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
10 00814008023134 AC-1416T-406 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
11 00814008023127 AC-1416T-405 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
12 00814008023110 AC-1416T-404 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
13 00814008023103 AC-1416T-403 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
14 00814008023097 AC-1416T-402 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
15 00814008023080 AC-1416T-401 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
16 00814008023073 AC-1416T-400 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
17 00814008023066 AC-1214T-415 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
18 00814008023059 AC-1214T-414 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
19 00814008023042 AC-1214T-413 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
20 00814008023035 AC-1214T-412 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
21 00814008023028 AC-1214T-411 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
22 00814008023011 AC-1214T-410 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
23 00814008023004 AC-1214T-409 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
24 00814008022991 AC-1214T-408 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
25 00814008022984 AC-1214T-407 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
26 00814008022977 AC-1214T-406 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
27 00814008022960 AC-1214T-405 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
28 00814008022953 AC-1214T-404 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
29 00814008022946 AC-1214T-403 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
30 00814008022939 AC-1214T-402 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
31 00814008022922 AC-1214T-401 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
32 00814008022915 AC-1214T-400 Instrument, Rasp, Anterior Cervical Interbody Fusion System (ACIF) nvc NVISION BIOMEDICAL TECHNOLOGIES, INC.
33 00812998049769 LSTS-SM0612-MSR LSTS-SM0612-MSR 4WEB Medical 4WEB MEDICAL
34 00812998049752 LSTS-SM0610-MSR LSTS-SM0610-MSR 4WEB Medical 4WEB MEDICAL
35 00812998049745 LSTS-SM0608-MSR LSTS-SM0608-MSR 4WEB Medical 4WEB MEDICAL
36 00812998048793 LSTS-000411 LSTS-000411 4WEB Medical 4WEB MEDICAL
37 00812998048786 LSTS-000410 LSTS-000410 4WEB Medical 4WEB MEDICAL
38 00812998046607 LSTS-300400 LSTS-300400 4WEB Medical 4WEB MEDICAL
39 00812998046591 LSTS-200400 LSTS-200400 4WEB Medical 4WEB MEDICAL
40 00812998046584 LSTS-100400 LSTS-100400 4WEB Medical 4WEB MEDICAL
41 00812998046386 CSTS-000019 CSTS-000019 4WEB Medical 4WEB MEDICAL
42 00812998043392 LSTS-000405 LSTS-000405 4WEB Medical 4WEB MEDICAL
43 00812998040414 LSTS-000400 LSTS-000400 4WEB Medical 4WEB MEDICAL
44 00812998033928 CSTS-MDXX12-RS CSTS-MDXX12-RS 4WEB Medical 4WEB MEDICAL
45 00812998033911 CSTS-MDXX11-RS CSTS-MDXX11-RS 4WEB Medical 4WEB MEDICAL
46 00812998033904 CSTS-MDXX10-RS CSTS-MDXX10-RS 4WEB Medical 4WEB MEDICAL
47 00812998033898 CSTS-MDXX09-RS CSTS-MDXX09-RS 4WEB Medical 4WEB MEDICAL
48 00812998033881 CSTS-MDXX08-RS CSTS-MDXX08-RS 4WEB Medical 4WEB MEDICAL
49 00812998033874 CSTS-MDXX07-RS CSTS-MDXX07-RS 4WEB Medical 4WEB MEDICAL
50 00812998033867 CSTS-MDXX06-RS CSTS-MDXX06-RS 4WEB Medical 4WEB MEDICAL