No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | M697N600016301 | N60001630 | 1/4" BOX CONNECT/JACOBS CHUCK ADAPTER | HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT | 1 | Silex Sacroiliac Joint Fusion System | |
2 | M697N600004721 | N60000472 | Capless Screw System Ratcheting T-handle | HXC | WRENCH | 1 | Silex Sacroiliac Joint Fusion System | |
3 | M697CN6000441 | CN60-0044 | Specialty Cervical Distractor - Calix | HWB | EXTRACTOR | 1 | Calix Spinal Implant System | |
4 | M697C07902661 | C079-0266 | SPECIAL 12.5mm GRAFT FUNNEL ASSEMBLY | HXG | Tamp | 1 | Silex Sacroiliac Joint Fusion System | |
5 | M697C07902651 | C079-0265 | SPECIAL GRAFT TAMP | HXG | Tamp | 1 | Silex Sacroiliac Joint Fusion System | |
6 | M697C07902641 | C079-0264 | SPECIAL 7mm ADJUSTMENT IMPLANT DRIVER, CANNULATED | HXX | Screwdriver | 1 | Silex Sacroiliac Joint Fusion System | |
7 | M697C07902631 | C079-0263 | Special Guide Handle Assembly, Soft Tissue Shield | FZX | Guide, Surgical, Instrument | 1 | Silex Sacroiliac Joint Fusion System | |
8 | M697C07902621 | C079-0262 | Special Instrument 8mm x 25cm Bone Funnel Assembly | HXG | Tamp | 1 | Silex Sacroiliac Joint Fusion System | |
9 | M697C07902611 | C079-0261 | Special Instrument 8mm x 25cm Tamp Assembly | HXG | Tamp | 1 | Silex Sacroiliac Joint Fusion System | |
10 | M697C07900581 | C079-0058 | Specialty Silex 800 mm Trocar Steinman Pin w/breakaway pt @500mm | GDF | GUIDE, NEEDLE, SURGICAL | Silex Sacroiliac Joint Fusion System | ||
11 | M697C07900571 | C079-0057 | Specialty Silex Aggressive Tip 7mm drill | HTW | BIT, DRILL | 1 | Silex Sacroiliac Joint Fusion System | |
12 | M697C07900561 | C079-0056 | Specialty Silex Aggressive Tip 12.5mm Drill | HTW | Bit, Drill | 1 | Silex Sacroiliac Joint Fusion System | |
13 | M697C07900551 | C079-0055 | Specialty Silex 800 mm Steinmann pin case | GDF | GUIDE, NEEDLE, SURGICAL | 1 | Silex Sacroiliac Joint Fusion System | |
14 | M697C07900531 | C079-0053 | Silex Tissue Spreader Assembly | EMF | KNIFE, SURGICAL | 1 | Silex Sacroiliac Joint Fusion System | |
15 | M697C07900521 | C079-0052 | Specialty Fully Threaded 2.4mm x 300mm Steinmann Pin | GDF | GUIDE, NEEDLE, SURGICAL | 1 | Silex Sacroiliac Joint Fusion System | |
16 | M697C07900501 | C079-0050 | Specialty Jamshidi Awl Insert | HWJ | AWL | 1 | Silex Sacroiliac Joint Fusion System | |
17 | M697C07900491 | C079-0049 | Specialty Cannulated Awl | HWJ | AWL | 1 | Silex Sacroiliac Joint Fusion System | |
18 | M697C07900481 | C079-0048 | Specialty 800mm Long Steinmann Pinn | GDF | GUIDE, NEEDLE, SURGICAL | 1 | Silex Sacroiliac Joint Fusion System | |
19 | M697C07900441 | C079-0044 | Specialty Silex Drill | HTW | BIT, DRILL | 1 | Silex Sacroiliac Joint Fusion System | |
20 | M697C07900411 | C079-0041 | SPECIALTY THREADED STEINMANN PIN 2.4 X 500MM TROCAR TIP | GDF | GUIDE, NEEDLE, SURGICAL | 1 | Silex Sacroiliac Joint Fusion System | |
21 | M697C07900391 | C079-0039 | SPECIALTY #3 STS MORE AGGRESSIVE TIP | FZX | Guide, surgical, instrument | 1 | Silex Sacroiliac Joint Fusion System | |
22 | M697C07900381 | C079-0038 | SPECIALTY #2 STS MORE AGGRESSIVE TIP | HWX | TAP, BONE | 1 | Silex Sacroiliac Joint Fusion System | |
23 | M697C07900371 | C079-0037 | SPECIALTY SILEX WASHER REMOVAL TOOL ASSEMBLY | HWB | EXTRACTOR | 1 | Silex Sacroiliac Joint Fusion System | |
24 | M697C07900301 | C079-0030 | SPECIALTY GUIDE TUBE HANDLE | FZX | Guide, surgical, instrument | 1 | Silex Sacroiliac Joint Fusion System | |
25 | M697C07900271 | C079-0027 | Specialty Silex 12.5mm Tap Aggressive Tip | HWX | TAP, BONE | 1 | Silex Sacroiliac Joint Fusion System | |
26 | M697C07900261 | C079-0026 | CUSTOM IMPACTION DRIVER | HWA | IMPACTOR | 1 | Silex Sacroiliac Joint Fusion System | |
27 | M697C07900251 | C079-0025 | Specialty Silex #3 STS | FZX | Guide, surgical, instrument | 1 | Silex Sacroiliac Joint Fusion System | |
28 | M697C07900241 | C079-0024 | Specialty Silex #2 STS | FZX | Guide, surgical, instrument | 1 | Silex Sacroiliac Joint Fusion System | |
29 | M697C07900111 | C079-0011 | SPECIALTY 12.5 mm IMPLANT DRIVER | HXX | SCREWDRIVER | 1 | Silex Sacroiliac Joint Fusion System | |
30 | M697C07900031 | C079-0003 | SPECIAL 12.5MM TAP | HWX | TAP, BONE | 1 | Silex Sacroiliac Joint Fusion System | |
31 | M697C07900021 | C079-0002 | SPECIAL 12.5MM DRILL | HTW | BIT, DRILL | 1 | Silex Sacroiliac Joint Fusion System | |
32 | M697C07900011 | C079-0001 | CUSTOM #1 SOFT TISSUE SHIELD | FZX | Guide, surgical, instrument | 1 | Silex Sacroiliac Joint Fusion System | |
33 | M697C07600061 | C076-0006 | Specialty Luer Lock adapter for Osteosponge putty syringe | MJG | DEVICE, PERCUTANEOUS, BIOPSY | 1 | Zyfix Spinal Facet Screw System | |
34 | M697C07600051 | C076-0005 | Specialty Luer Lock adapter for Osteosponge putty syringe | MJG | DEVICE, PERCUTANEOUS, BIOPSY | 1 | Zyfix Spinal Facet Screw System | |
35 | M697C07600041 | C076-0004 | Specialty Luer Lock adapter for Osteosponge putty syringe | MJG | DEVICE, PERCUTANEOUS, BIOPSY | 1 | Zyfix Spinal Facet Screw System | |
36 | M697X07900341 | X079-0034 | 7mm DRILL BIT, CANNULATED | HTW | BIT, DRILL | 1 | Silex Sacroiliac Joint Fusion System | |
37 | 00849777011969 | C024-0025-PTYV | ONE (1) PACKAGE - CONTAINING 2.5cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | CuriGraft DBM Putty, 2.5cc | |
38 | 00849777011921 | IFLX-CR-05 | ONE (1) PACKAGE - CONTAINING 5.0cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | Influx Plus Crunch 5.0cc - Syringe | |
39 | 00849777011754 | MFC-5 | ONE (1) PACKAGE - CONTAINING 5.0cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | MAXX™ Fuse DBM Putty with Chips 5cc | |
40 | 00849777011570 | X055-0045 | 10.0cc (Jar) | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | DMB Putty 10.0cc | |
41 | 00849777010535 | IS59P025 | ONE (1) PACKAGE - CONTAINING 2.5cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | DBM Putty 2.5cc-Syringe | |
42 | 00849777010184 | BX-600-005-M | ONE (1) PACKAGE - CONTAINING 0.5cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | DBM Putty 0.5cc | |
43 | 00849777009683 | BM895005 | ONE (1) PACKAGE - CONTAINING 0.5cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | DBM Putty 0.5cc | |
44 | 00849777008778 | 27800418 | ONE (1) PACKAGE - CONTAINING 5.0cc | MQV,MBP | Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | 2 | Reficio DBM Putty 5cc | |
45 | 00849777008761 | 27800218 | ONE (1) PACKAGE - CONTAINING 1.0cc | MQV,MBP | Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | 2 | Reficio DBM Putty 1cc | |
46 | 00849777008532 | DU-25PS | ONE (1) PACKAGE - CONTAINING 2.5cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | DBM Putty 2.5cc Syringe | |
47 | 00849777008372 | X090-0015-PT0.5CCJ | ONE (1) PACKAGE - CONTAINING 0.5cc | MBP,MQV | Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, C Filler, Bone Void, Osteoinduction (W/O Human Growth Factor),Filler, Bone Void, Calcium Compound | 2 | Axograft DBM Putty 0.5cc - Jar | |
48 | 00849777008136 | BXS-600-025-M | ONE (1) PACKAGE - CONTAINING 2.5cc | MQV,MBP | Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | 2 | DBM Putty 2.5cc in a Syringe | |
49 | 00849777007733 | NUX-02P | ONE (1) PACKAGE - CONTAINING 2.5cc | MQV,MBP | Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | 2 | DBM Putty 2.5cc in a Syringe | |
50 | 00849777007474 | XT-309025 | 2.5cc | MQV,MBP | Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Filler, Bone Void, Calcium Compound,Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) | 2 | KBM STERILE PUTTY |
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 | 00812998044399 | CSTS-000022 | CSTS-000022 | 4WEB Medical | 4WEB MEDICAL | |
18 | 00812998044382 | CSTS-000021 | CSTS-000021 | 4WEB Medical | 4WEB MEDICAL | |
19 | 00812998033959 | CSTS-000015 | CSTS-000015 | 4WEB Medical | 4WEB MEDICAL | |
20 | 00812998033607 | CSTS-MD0704 | CSTS-MD0704 | 4WEB Medical | 4WEB MEDICAL | |
21 | 00812998033591 | CSTS-MD0004 | CSTS-MD0004 | 4WEB Medical | 4WEB MEDICAL | |
22 | 00812998033584 | CSTS-SM0704 | CSTS-SM0704 | 4WEB Medical | 4WEB MEDICAL | |
23 | 00812998033577 | CSTS-SM0004 | CSTS-SM0004 | 4WEB Medical | 4WEB MEDICAL | |
24 | 00812998021789 | CSTS-000012 | CSTS-000012 | 4WEB Medical | 4WEB MEDICAL | |
25 | 00812998021772 | CSTS-000011 | CSTS-000011 | 4WEB Medical | 4WEB MEDICAL | |
26 | 00812998020324 | CSTS-SM0712 | CSTS-SM0712 | 4WEB Medical | 4WEB MEDICAL | |
27 | 00812998020317 | CSTS-SM0711 | CSTS-SM0711 | 4WEB Medical | 4WEB MEDICAL | |
28 | 00812998020300 | CSTS-SM0710 | CSTS-SM0710 | 4WEB Medical | 4WEB MEDICAL | |
29 | 00812998020294 | CSTS-SM0709 | CSTS-SM0709 | 4WEB Medical | 4WEB MEDICAL | |
30 | 00812998020287 | CSTS-SM0708 | CSTS-SM0708 | 4WEB Medical | 4WEB MEDICAL | |
31 | 00812998020270 | CSTS-SM0707 | CSTS-SM0707 | 4WEB Medical | 4WEB MEDICAL | |
32 | 00812998020263 | CSTS-SM0706 | CSTS-SM0706 | 4WEB Medical | 4WEB MEDICAL | |
33 | 00812998020256 | CSTS-SM0705 | CSTS-SM0705 | 4WEB Medical | 4WEB MEDICAL | |
34 | 00812998020249 | CSTS-SM0012 | CSTS-SM0012 | 4WEB Medical | 4WEB MEDICAL | |
35 | 00812998020232 | CSTS-SM0011 | CSTS-SM0011 | 4WEB Medical | 4WEB MEDICAL | |
36 | 00812998020225 | CSTS-SM0010 | CSTS-SM0010 | 4WEB Medical | 4WEB MEDICAL | |
37 | 00812998020218 | CSTS-SM0009 | CSTS-SM0009 | 4WEB Medical | 4WEB MEDICAL | |
38 | 00812998020201 | CSTS-SM0008 | CSTS-SM0008 | 4WEB Medical | 4WEB MEDICAL | |
39 | 00812998020195 | CSTS-SM0007 | CSTS-SM0007 | 4WEB Medical | 4WEB MEDICAL | |
40 | 00812998020188 | CSTS-SM0006 | CSTS-SM0006 | 4WEB Medical | 4WEB MEDICAL | |
41 | 00812998020171 | CSTS-SM0005 | CSTS-SM0005 | 4WEB Medical | 4WEB MEDICAL | |
42 | 00812998020164 | CSTS-MD0712 | CSTS-MD0712 | 4WEB Medical | 4WEB MEDICAL | |
43 | 00812998020157 | CSTS-MD0711 | CSTS-MD0711 | 4WEB Medical | 4WEB MEDICAL | |
44 | 00812998020140 | CSTS-MD0710 | CSTS-MD0710 | 4WEB Medical | 4WEB MEDICAL | |
45 | 00812998020133 | CSTS-MD0709 | CSTS-MD0709 | 4WEB Medical | 4WEB MEDICAL | |
46 | 00812998020126 | CSTS-MD0708 | CSTS-MD0708 | 4WEB Medical | 4WEB MEDICAL | |
47 | 00812998020119 | CSTS-MD0707 | CSTS-MD0707 | 4WEB Medical | 4WEB MEDICAL | |
48 | 00812998020102 | CSTS-MD0706 | CSTS-MD0706 | 4WEB Medical | 4WEB MEDICAL | |
49 | 00812998020096 | CSTS-MD0705 | CSTS-MD0705 | 4WEB Medical | 4WEB MEDICAL | |
50 | 00812998020089 | CSTS-MD0012 | CSTS-MD0012 | 4WEB Medical | 4WEB MEDICAL |