| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00841523155903 | Tesera-k ALIF | 2167-002-001 | Straight Punch Awl | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 2 | 00841523155606 | Tesera-k ALIF | 2167-000-056 | Size 4 Cup Curette | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 3 | 00841523155590 | Tesera-k ALIF | 2167-000-054 | Size 2 Cup Curette | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 4 | 00841523160488 | Tesera-k ALIF | 2167-013-001 | Angled Cover Plate Inserter | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 5 | 00841523155583 | Tesera-k ALIF | 2167-000-031 | Endplate Perforator Tool | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 6 | 00841523160471 | Tesera-k ALIF | 2167-011-003 | Angled Tesera-k ALIF Cage Inserter | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 7 | 00841523155699 | Tesera-k ALIF | 2167-000-074 | 13mm Endplate Rasp | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 8 | 00841523155576 | Tesera-k ALIF | 2167-000-030 | 90° Ball Tip Probe | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 9 | 00841523158393 | Tesera-k ALIF | 2167-012-015 | Angled Retaining Hex Driver | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 10 | 00841523158355 | Tesera-k ALIF | 3167-006-000 | 27x24 Tesera-k A ALIF Instrument Case | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 11 | 00841523155569 | Tesera-k ALIF | 2167-000-027 | 6mm Kerrison Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 12 | 00841523158348 | Tesera-k ALIF | 2168-442-221 | Tesera-k ALIF, 42W X 32D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 13 | 00841523158331 | Tesera-k ALIF | 2168-442-219 | Tesera-k ALIF, 42W X 32D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 14 | 00841523158324 | Tesera-k ALIF | 2168-438-021 | Tesera-k ALIF, 38W X 30D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 15 | 00841523158317 | Tesera-k ALIF | 2168-438-019 | Tesera-k ALIF, 38W X 30D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 16 | 00841523158300 | Tesera-k ALIF | 2168-434-821 | Tesera-k ALIF, 34W X 28D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 17 | 00841523158294 | Tesera-k ALIF | 2168-434-819 | Tesera-k ALIF, 34W X 28D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 18 | 00841523155552 | Tesera-k ALIF | 2167-000-026 | 3mm Kerrison Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 19 | 00841523158287 | Tesera-k ALIF | 2168-434-817 | Tesera-k ALIF, 34W X 28D, 17mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 20 | 00841523158270 | Tesera-k ALIF | 2168-431-621 | Tesera-k ALIF, 31W X 26D, 21mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 21 | 00841523158263 | Tesera-k ALIF | 2168-431-619 | Tesera-k ALIF, 31W X 26D, 19mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 22 | 00841523157860 | Tesera-k ALIF | 3167-004-000 | Tesera-k ALIF Trial Case | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 23 | 00841523158256 | Tesera-k ALIF | 2168-431-617 | Tesera-k ALIF, 31W X 26D, 17mm, 28° Broach | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 24 | 00841523158249 | Tesera-k ALIF | 2167-442-221 | Tesera-k ALIF, 42W X 32D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 25 | 00841523158232 | Tesera-k ALIF | 2167-442-219 | Tesera-k ALIF, 42W X 32D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 26 | 00841523158225 | Tesera-k ALIF | 2167-438-021 | Tesera-k ALIF, 38W X 30D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 27 | 00841523158218 | Tesera-k ALIF | 2167-438-019 | Tesera-k ALIF, 38W X 30D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 28 | 00841523158201 | Tesera-k ALIF | 2167-434-821 | Tesera-k ALIF, 34W X 28D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 29 | 00841523155545 | Tesera-k ALIF | 2167-000-025 | 8mm Pituitary Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 30 | 00841523158195 | Tesera-k ALIF | 2167-434-819 | Tesera-k ALIF, 34W X 28D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 31 | 00841523155538 | Tesera-k ALIF | 2167-000-024 | 4mm Pituitary Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 32 | 00841523158188 | Tesera-k ALIF | 2167-434-817 | Tesera-k ALIF, 34W X 28D, 17mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 33 | 00841523158171 | Tesera-k ALIF | 2167-431-621 | Tesera-k ALIF, 31W X 26D, 21mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 34 | 00841523158164 | Tesera-k ALIF | 2167-431-619 | Tesera-k ALIF, 31W X 26D, 19mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 35 | 00841523155521 | Tesera-k ALIF | 2167-000-023 | 10mm Sypert Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 36 | 00841523158157 | Tesera-k ALIF | 2167-431-617 | Tesera-k ALIF, 31W X 26D, 17mm, 28° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 37 | 00841523158140 | Tesera-k ALIF | 2167-134-809 | Tesera-k ALIF, 34W X 28D, 9.5mm, 12° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 38 | 00841523158133 | Tesera-k ALIF | 2167-131-609 | Tesera-k ALIF, 31W X 26D, 9.5mm, 12° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 39 | 00841523158126 | Tesera-k ALIF | 2167-042-209 | Tesera-k ALIF, 42W X 32D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 40 | 00841523155514 | Tesera-k ALIF | 2167-000-022 | 5mm Sypert Rongeur | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 41 | 00841523155507 | Tesera-k ALIF | 2167-000-021 | Scalpel Handle | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 42 | 00841523155491 | Tesera-k ALIF | 2167-000-004 | 42W x 32D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 43 | 00841523158119 | Tesera-k ALIF | 2167-038-009 | Tesera-k ALIF, 38W X 30D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 44 | 00841523158102 | Tesera-k ALIF | 2167-034-809 | Tesera-k ALIF, 34W X 28D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 45 | 00841523158096 | Tesera-k ALIF | 2167-031-609 | Tesera-k ALIF, 31W X 26D, 9.5mm, 7° Trial | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 46 | 00841523158072 | Tesera-k ALIF | 2167-000-000 | 27W x 24D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 47 | 00841523158065 | Tesera-k ALIF | 2167-001-008 | Tesera-k A ALIF 27W x 24D Oblique Cage Inserter Tip | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 48 | 00841523155484 | Tesera-k ALIF | 2167-000-003 | 38W x 30D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 49 | 00841523158058 | Tesera-k ALIF | 2167-001-007 | Tesera-k A ALIF Oblique Cage Inserter Tip | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| 50 | 00841523155477 | Tesera-k ALIF | 2167-000-002 | 34W x 28D Paddle Sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Kyocera Medical Technologies, Inc. |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00813210020856 | CIC2-10-12-00 | The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. | VariLift-C | WENZEL SPINE, INC. | |
| 2 | 00813210020849 | CIC2-09-12-00 | The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. | VariLift-C | WENZEL SPINE, INC. | |
| 3 | 00813210020832 | CIC2-08-12-00 | The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. | VariLift-C | WENZEL SPINE, INC. | |
| 4 | 00813210020788 | CIC2-A743 | Expander | VariLift-C | WENZEL SPINE, INC. | |
| 5 | 00813210020771 | CIC2-A742 | Retainer | VariLift-C | WENZEL SPINE, INC. | |
| 6 | 00813210020764 | CIC2-A741 | Inserter | VariLift-C | WENZEL SPINE, INC. | |
| 7 | 00813210020719 | CIC1-A743-C01 | Expansion Wrench, T-Handle | VariLift-C | WENZEL SPINE, INC. | |
| 8 | 00813210020702 | CIC1-A741-C01 | Insertion Wrench, T-Handle | VariLift-C | WENZEL SPINE, INC. | |
| 9 | 00813210020252 | CIC1-A747 | Removal Screwdriver | VariLift-C | WENZEL SPINE, INC. | |
| 10 | 00813210020221 | CIC1-A743 | Expansion Wrench | VariLift-C | WENZEL SPINE, INC. | |
| 11 | 00813210020214 | CIC1-A742 | Locking Wrench | VariLift-C | WENZEL SPINE, INC. | |
| 12 | 00813210020207 | CIC1-A741 | Insertion Wrench | VariLift-C | WENZEL SPINE, INC. | |
| 13 | 00813210020061 | CIC1-9.0-12-00 | The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. | VariLift-C | WENZEL SPINE, INC. | |
| 14 | 00813210020054 | CIC1-7.5-12-00 | The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. | VariLift-C | WENZEL SPINE, INC. | |
| 15 | 00813210020047 | CIC1-9.0-12-BP | The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. | VariLift-C | WENZEL SPINE, INC. | |
| 16 | 00813210020030 | CIC1-7.5-12-BP | The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. | VariLift-C | WENZEL SPINE, INC. | |
| 17 | 00812998046263 | CSTS-SA-ML0000 | CSTS-SA-ML0000 | 4WEB Medical | 4WEB MEDICAL | |
| 18 | 00812998046232 | CSTS-SA-MLMD10 | CSTS-SA-MLMD10 | 4WEB Medical | 4WEB MEDICAL | |
| 19 | 00812998046225 | CSTS-SA-MLMD09 | CSTS-SA-MLMD09 | 4WEB Medical | 4WEB MEDICAL | |
| 20 | 00812998046218 | CSTS-SA-MLMD08 | CSTS-SA-MLMD08 | 4WEB Medical | 4WEB MEDICAL | |
| 21 | 00812998046201 | CSTS-SA-MLMD07 | CSTS-SA-MLMD07 | 4WEB Medical | 4WEB MEDICAL | |
| 22 | 00812998046195 | CSTS-SA-MLMD06 | CSTS-SA-MLMD06 | 4WEB Medical | 4WEB MEDICAL | |
| 23 | 00812998046188 | CSTS-SA-MLMD05 | CSTS-SA-MLMD05 | 4WEB Medical | 4WEB MEDICAL | |
| 24 | 00812998046157 | CSTS-SA-MLSM10 | CSTS-SA-MLSM10 | 4WEB Medical | 4WEB MEDICAL | |
| 25 | 00812998046140 | CSTS-SA-MLSM09 | CSTS-SA-MLSM09 | 4WEB Medical | 4WEB MEDICAL | |
| 26 | 00812998046133 | CSTS-SA-MLSM08 | CSTS-SA-MLSM08 | 4WEB Medical | 4WEB MEDICAL | |
| 27 | 00812998046126 | CSTS-SA-MLSM07 | CSTS-SA-MLSM07 | 4WEB Medical | 4WEB MEDICAL | |
| 28 | 00812998046119 | CSTS-SA-MLSM06 | CSTS-SA-MLSM06 | 4WEB Medical | 4WEB MEDICAL | |
| 29 | 00812998046102 | CSTS-SA-MLSM05 | CSTS-SA-MLSM05 | 4WEB Medical | 4WEB MEDICAL | |
| 30 | 00812998044399 | CSTS-000022 | CSTS-000022 | 4WEB Medical | 4WEB MEDICAL | |
| 31 | 00812998044382 | CSTS-000021 | CSTS-000021 | 4WEB Medical | 4WEB MEDICAL | |
| 32 | 00812998041527 | CSTS-SA-GD0012 | CSTS-SA-GD0012 | 4WEB Medical | 4WEB MEDICAL | |
| 33 | 00812998041510 | CSTS-SA-GD0011 | CSTS-SA-GD0011 | 4WEB Medical | 4WEB MEDICAL | |
| 34 | 00812998041503 | CSTS-SA-GD0010 | CSTS-SA-GD0010 | 4WEB Medical | 4WEB MEDICAL | |
| 35 | 00812998041497 | CSTS-SA-GD0009 | CSTS-SA-GD0009 | 4WEB Medical | 4WEB MEDICAL | |
| 36 | 00812998041480 | CSTS-SA-GD0008 | CSTS-SA-GD0008 | 4WEB Medical | 4WEB MEDICAL | |
| 37 | 00812998041473 | CSTS-SA-GD0007 | CSTS-SA-GD0007 | 4WEB Medical | 4WEB MEDICAL | |
| 38 | 00812998041466 | CSTS-SA-GD0006 | CSTS-SA-GD0006 | 4WEB Medical | 4WEB MEDICAL | |
| 39 | 00812998041459 | CSTS-SA-GD0005 | CSTS-SA-GD0005 | 4WEB Medical | 4WEB MEDICAL | |
| 40 | 00812998039401 | CSCR-3816-SD-SP | CSCR-3816-SD-SP | 4WEB Medical | 4WEB MEDICAL | |
| 41 | 00812998039395 | CSCR-3814-SD-SP | CSCR-3814-SD-SP | 4WEB Medical | 4WEB MEDICAL | |
| 42 | 00812998039388 | CSCR-3812-SD-SP | CSCR-3812-SD-SP | 4WEB Medical | 4WEB MEDICAL | |
| 43 | 00812998039371 | CSCR-3514-SD-SP | CSCR-3514-SD-SP | 4WEB Medical | 4WEB MEDICAL | |
| 44 | 00812998039364 | CSCR-3512-SD-SP | CSCR-3512-SD-SP | 4WEB Medical | 4WEB MEDICAL | |
| 45 | 00812998039357 | CSCR-3816-SP | CSCR-3816-SP | 4WEB Medical | 4WEB MEDICAL | |
| 46 | 00812998039340 | CSCR-3814-SP | CSCR-3814-SP | 4WEB Medical | 4WEB MEDICAL | |
| 47 | 00812998039333 | CSCR-3812-SP | CSCR-3812-SP | 4WEB Medical | 4WEB MEDICAL | |
| 48 | 00812998039326 | CSCR-3516-SP | CSCR-3516-SP | 4WEB Medical | 4WEB MEDICAL | |
| 49 | 00812998039319 | CSCR-3514-SP | CSCR-3514-SP | 4WEB Medical | 4WEB MEDICAL | |
| 50 | 00812998039302 | CSCR-3512-SP | CSCR-3512-SP | 4WEB Medical | 4WEB MEDICAL |