No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00840019910224 | 26-221000-12 | 26-221000-12 | Wide PLIF Cage Peek 0 degree 22 x 10 X 12 | KWQ,MAX | Appliance, Fixation, Spinal Intervertebral Body,Intervertebral Fusion Device Wit Appliance, Fixation, Spinal Intervertebral Body,Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | ShurFit Interbody Deviceem |
2 | 00840019926027 | 43-2100-00 | 43-2100-00 | Medial Blade Rack Assembly | GAD | Retractor | 1 | MD-Max ULIF |
3 | 00840019932684 | 62-BK-0103 | 62-BK-0103 | ACIF 2C Instrument BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
4 | 00840019932677 | 62-BK-0102 | 62-BK-0102 | ACIF 2C Instrument BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
5 | 00840019937191 | 39-BK-0703 | 39-BK-0703 | Implant Kit: Std + Red (Ti) | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | Implant Kit: Std + Red (Ti) |
6 | 00840019932660 | 62-BK-0101 | 62-BK-0101 | ACIF 2C Instrument BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
7 | 00840019936972 | 43-8700-CA | 43-8700-CA | MD-Max™ Pedicle Screw System Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
8 | 00840019936965 | 43-8600-CA | 43-8600-CA | MD-Max™ Triple Lead System Implant Case | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | MD-Max ULIF |
9 | 00840019936958 | 43-8500-CA | 43-8500-CA | MD-Max™ Implant Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
10 | 00840019936941 | 43-8200-CA | 43-8200-CA | MD-Max™ Triple Lead MIS Instrument Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
11 | 00840019936934 | 43-8100-CA | 43-8100-CA | MD-Max™ Triple Lead System Instrument Case | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
12 | 00840019936927 | 43-8000-CA | 43-8000-CA | MD-Max™ ULIF Retractor Instrument Kit | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
13 | 00840019932707 | ACIFXX-XXP-2C-CC | ACIFXX-XXP-2C-CC | ACIF 2C Wide Kit Case BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
14 | 00840019932691 | 62-BK-0601 | 62-BK-0601 | ACIF 2C Wide Kit Case BOM | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
15 | 00840019926089 | 43-5000 | 43-5000 | Lumitex Light Source | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
16 | 00840019926218 | 43-8700 | 43-8700 | MD-Max™ Pedicle Screw System Case - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
17 | 00840019926201 | 43-8600 | 43-8600 | MD-Max™ Triple Lead System Implant Tray - Empty | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | MD-Max ULIF |
18 | 00840019926195 | 43-8550 | 43-8550 | MD-Max™ Implant Case - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
19 | 00840019926188 | 43-8200 | 43-8200 | MD-Max™ Triple Lead MIS Instrument Case - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
20 | 00840019926171 | 43-8100 | 43-8100 | MD-Max™ Triple Lead System Instrument Tray - Empty | MNI,MNH | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation | 2 | MD-Max ULIF |
21 | 00840019926164 | 43-8050 | 43-8050 | MD-Max™ ULIF Retractor Instrument Case - Empty | MNH,MNI | Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation | 2 | MD-Max ULIF |
22 | 00840019926157 | 48-9018 | 48-9018 | MD-Max Bottle Cap Reducer | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
23 | 00840019926140 | 43-6200 | 43-6200 | Contralateral Sleeve Assembly | GAD | Retractor | 1 | MD-Max ULIF |
24 | 00840019926133 | 43-6100-100 | 43-6100-100 | Ipsilateral Sleeve Assembly, 100mm | GAD | Retractor | 1 | MD-Max ULIF |
25 | 00840019926126 | 43-6100-080 | 43-6100-080 | Ipsilateral Sleeve Assembly, 80mm | GAD | Retractor | 1 | MD-Max ULIF |
26 | 00840019926119 | 43-6100-060 | 43-6100-060 | Ipsilateral Sleeve Assembly, 60mm | GAD | Retractor | 1 | MD-Max ULIF |
27 | 00840019926102 | 43-6100-040 | 43-6100-040 | Ipsilateral Sleeve Assembly, 40mm | GAD | Retractor | 1 | MD-Max ULIF |
28 | 00840019926096 | 43-6000 | 43-6000 | Bilateral Retractor Assembly | GAD | Retractor | 1 | MD-Max ULIF |
29 | 00840019926072 | 43-4100-85 | 43-4100-85 | 8.5mm MD-Max Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
30 | 00840019926065 | 43-4100-75 | 43-4100-75 | 7.5mm MD-Max™ Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
31 | 00840019926058 | 43-4100-65 | 43-4100-65 | 6.5mm MD-Max™ Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
32 | 00840019926041 | 43-4100-55 | 43-4100-55 | 5.5mm MD-Max™ Triple Lead Tap | HWX | Tap, Bone | 1 | MD-Max ULIF |
33 | 00840019926034 | 43-2200-00 | 43-2200-00 | Medial Blade Bar | GAD | Retractor | 1 | MD-Max ULIF |
34 | 00840019926010 | 43-2000-110 | 43-2000-110 | Medial Retractor Blade, 110 mm | GAD | Retractor | 1 | MD-Max ULIF |
35 | 00840019926003 | 43-2000-100 | 43-2000-100 | Medial Retractor Blade, 100 mm | GAD | Retractor | 1 | MD-Max ULIF |
36 | 00840019925990 | 43-2000-090 | 43-2000-090 | Medial Retractor Blade, 90 mm | GAD | Retractor | 1 | MD-Max ULIF |
37 | 00840019925983 | 43-2000-080 | 43-2000-080 | Medial Retractor Blade, 80 mm | GAD | Retractor | 1 | MD-Max ULIF |
38 | 00840019925976 | 43-2000-070 | 43-2000-070 | Medial Retractor Blade, 70 mm | GAD | Retractor | 1 | MD-Max ULIF |
39 | 00840019925969 | 43-2000-060 | 43-2000-060 | Medial Retractor Blade, 60 mm | GAD | Retractor | 1 | MD-Max ULIF |
40 | 00840019925952 | 43-2000-050 | 43-2000-050 | Medial Retractor Blade, 50 mm | GAD | Retractor | 1 | MD-Max ULIF |
41 | 00840019925945 | 43-2000-040 | 43-2000-040 | Medial Retractor Blade, 40 mm | GAD | Retractor | 1 | MD-Max ULIF |
42 | 00840019925938 | 43-1629 | 43-1629 | Hexdriver | HXX | Screwdriver | 1 | MD-Max ULIF |
43 | 00840019925921 | 43-1545 | 43-1545 | Drill, Pedicle Targeting | HTW | Bit, Drill | 1 | MD-Max ULIF |
44 | 00840019925907 | 43-0552 | 43-0552 | Torque Limiting T-Handle 36 in-lbs | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
45 | 00840019925891 | 43-0080 | 43-0080 | Reusable Light Cable-Lumitex | LXH | Orthopedic Manual Surgical Instrument | 1 | MD-Max ULIF |
46 | 00840019921077 | 62-NR-5007 | 62-NR-5007 | ACIF Rasp, 18 x 15 x 7 | HTR | Rasp | 1 | ShurFit ACIF 2C |
47 | 00840019921428 | 62-TN-1815-10 | 62-TN-1815-10 | ACIF Trial, 18 x 15 x 10 | HWT | Template | 1 | ShurFit ACIF 2C |
48 | 00840019921060 | 62-NR-5006 | 62-NR-5006 | ACIF Rasp, 18 x 15 x 6 | HTR | Rasp | 1 | ShurFit ACIF 2C |
49 | 00840019921480 | 62-SC-0103 | 62-SC-0103 | ACIF 2C Instrument Case - Expanded | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
50 | 00840019921473 | 62-SC-0102 | 62-SC-0102 | ACIF 2C Instrument Case - Expanded + Double Wide | ODP | Intervertebral Fusion Device With Bone Graft, Cervical | 2 | ShurFit ACIF 2C |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00817577022782 | 2100-1015 | 2100-1015 | CUSTOM MAGLAMORY INSTR. | NA | EXACTECH, INC. |
2 | 00817121000198 | 1011180 | 1011180 | The Cor-Valv Cable is intended to be used with the corresponding CORONEO Cor-Val The Cor-Valv Cable is intended to be used with the corresponding CORONEO Cor-Valv system retractor for retraction of heart tissue during cardiac surgery. This product is provided sterile in a sealed package, and consists one(1) cable that is single-use and disposable held by a plastic insert. | Cor-Valv Atrial Retractor Cables with Fitting | CORONEO INC |
3 | 00816728021520 | A175WTSE | A175WTSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
4 | 00816728021513 | A175WSE | A175WSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
5 | 00816728021506 | A175TSE | A175TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
6 | 00816728021490 | 175mm Retractor | A175SE | LT Adapt Smoke Evacuation Retractor, 175mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
7 | 00816728021483 | A155WTSE | A155WTSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
8 | 00816728021476 | A155WSE | A155WSE | LT Adapt Smoke Evacuation Retractor, 155mm, Wide | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
9 | 00816728021469 | A155TSE | A155TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
10 | 00816728021452 | 155mm Retractor | A155SE | LT Adapt Smoke Evacuation Retractor, 155mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
11 | 00816728021445 | A135WTSE | A135WTSE | LT Adapt Smoke Evacuation Retractor, 135mm, Wide, Teeth | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
12 | 00816728021438 | A135WSE | A135WSE | LT Adapt Smoke Evacuation Retractor, 135mm, Wide | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
13 | 00816728021421 | A135TSE | A135TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
14 | 00816728021414 | 135mm Retractor | A135SE | LT Adapt Smoke Evacuation Retractor, 135mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
15 | 00816728021407 | A90WTSE | A90WTSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
16 | 00816728021391 | A90WSE | A90WSE | LT Adapt Smoke Evacuation Retractor, 90mm, Wide | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
17 | 00816728021384 | A90TSE | A90TSE | Intended to provide tissue retraction and surgical site illumination from a high Intended to provide tissue retraction and surgical site illumination from a high intensity light source. Additionally, the device is intended to remove smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system. | Eikon LT Adapt Smoke Evacuation | INVUITY, INC. |
18 | 00816728021377 | 90mm Retractor | A90SE | LT Adapt Smoke Evacuation Retractor, 90mm | Eikon LT Adapt Smoke Evacuation | STRYKER CORPORATION |
19 | 00816728021032 | C80R | C80R | LT Retractor, Rich, 80mm x 60mm | Eikon | STRYKER CORPORATION |
20 | 00816728021025 | C60R | C60R | LT Retractor, Rich, 60mm x 45mm | Eikon | STRYKER CORPORATION |
21 | 00816728021018 | C40R | C40R | LT Retractor, Rich, 40mm x 38mm | Eikon | STRYKER CORPORATION |
22 | 00816728021001 | C3550AN | C3550AN | LT Retractor, A-N, 35mm & 50mm | Eikon | STRYKER CORPORATION |
23 | 00816728020974 | 11109 | 11109 | Glenoid Retractor | N/A | STRYKER CORPORATION |
24 | 00816728020967 | E1SL | E1SL | Retractor, Standard, Long | Eiberg | STRYKER CORPORATION |
25 | 00816728020950 | E1S | E1S | Retractor, Standard | Eiberg | STRYKER CORPORATION |
26 | 00816728020844 | C175T | C175T | LT Retractor, 175 mm, Teeth | Eikon | STRYKER CORPORATION |
27 | 00816728020837 | C175 | C175 | LT Retractor, 175mm | Eikon | STRYKER CORPORATION |
28 | 00816728020820 | C135SH | C135SH | LT Retractor, 135mm, Sweetheart | Eikon | STRYKER CORPORATION |
29 | 00816728020813 | C135W | C135W | LT Retractor, 135mm, Wide | Eikon | STRYKER CORPORATION |
30 | 00816728020806 | C135WT | C135WT | LT Retractor, 135mm, Wide, Teeth | Eikon | STRYKER CORPORATION |
31 | 00816728020790 | C135T | C135T | LT Retractor, 135 mm, Teeth | Eikon | STRYKER CORPORATION |
32 | 00816728020783 | C135NT | C135NT | LT Retractor, 135 mm, Narrow, Teeth | Eikon | STRYKER CORPORATION |
33 | 00816728020776 | C135 | C135 | LT Retractor, 135 mm | Eikon | STRYKER CORPORATION |
34 | 00816728020769 | C135N | C135N | LT Retractor, 135mm, Narrow | Eikon | STRYKER CORPORATION |
35 | 00816728020752 | C90W | C90W | LT Retractor, 90 mm, Wide | Eikon | STRYKER CORPORATION |
36 | 00816728020745 | C90WT | C90WT | LT Retractor, 90 mm, Wide, Teeth | Eikon | STRYKER CORPORATION |
37 | 00816728020738 | C90T | C90T | LT Retractor, 90mm, Teeth | Eikon | STRYKER CORPORATION |
38 | 00816728020721 | C90NT | C90NT | LT Retractor, 90mm, Narrow, Teeth | Eikon | STRYKER CORPORATION |
39 | 00816728020714 | C90N | C90N | LT Retractor, 90mm, Narrow | Eikon | STRYKER CORPORATION |
40 | 00816728020707 | C90 | C90 | LT Retractor, 90mm | Eikon | STRYKER CORPORATION |
41 | 00816728020691 | C50T | C50T | LT Retractor, 50 mm, Teeth | Eikon | STRYKER CORPORATION |
42 | 00816728020684 | C50 | C50 | LT Retractor, 50 mm | Eikon | STRYKER CORPORATION |
43 | 00816728020677 | C40N | C40N | LT Retractor, 40mm, Narrow | Eikon | STRYKER CORPORATION |
44 | 00816728020660 | C40XN | C40XN | LT Retractor, 40 mm, Extra Narrow | Eikon | STRYKER CORPORATION |
45 | 00816728020554 | A38D | A38D | Deaver 38mm Wide Retractor | N/A | STRYKER CORPORATION |
46 | 00816728020547 | A25D | A25D | Deaver 25mm Wide Retractor | N/A | STRYKER CORPORATION |
47 | 00816728020493 | C3550ANXN | C3550ANXN | LT Retractor, A-N, 35mm & 50mm Extra Narrow | Eikon | STRYKER CORPORATION |
48 | 00816728020486 | C3550ANN | C3550ANN | LT Retractor, A-N, 35mm & 50mm Narrow | Eikon | STRYKER CORPORATION |
49 | 00812998040186 | LSTS-000022 | LSTS-000022 | 4WEB Medical | 4WEB MEDICAL | |
50 | 00812998032303 | PSTS-000501 | PSTS-000501 | 4WEB Medical | 4WEB MEDICAL |