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 | 03700757200803 | KIT0708 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his | spineEOS rod Template | ONEFIT MEDICAL |
2 | 03700757200797 | KIT0707 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
3 | 03700757200780 | KIT0706 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
4 | 03700757200773 | KIT0705 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
5 | 03700757200766 | KIT0704 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
6 | 03700757200759 | KIT0703 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
7 | 03700757200650 | KIT0702 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
8 | 03700757200643 | KIT0701 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
9 | 03700386990014 | MWA255 | MWA255 | HUMERAL HEAD TRIAL | Aequalis Fracture | TORNIER |
10 | 03700386990007 | MWA254 | MWA254 | HUMERAL HEAD TRIAL | Aequalis Fracture | TORNIER |
11 | 03700386989834 | MWF339 | MWF339 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
12 | 03700386989827 | MWF337S | MWF337S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
13 | 03700386989810 | MWF337 | MWF337 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
14 | 03700386989759 | MWF255S | MWF255S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
15 | 03700386989742 | MWF255 | MWF255 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
16 | 03700386989735 | MWF254S | MWF254S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
17 | 03700386989728 | MWF254 | MWF254 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
18 | 03700386989711 | MWF237 | MWF237 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
19 | 03700386975547 | MWF355S | MWF355S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
20 | 03700386975530 | MWF355 | MWF355 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
21 | 03700386975523 | MWF354S | MWF354S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
22 | 03700386975516 | MWF354 | MWF354 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
23 | 03700386975509 | MWF353S | MWF353S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
24 | 03700386975493 | MWF353 | MWF353 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
25 | 03700386975486 | MWF352S | MWF352S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
26 | 03700386975479 | MWF352 | MWF352 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
27 | 03700386975462 | MWF351S | MWF351S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
28 | 03700386975455 | MWF351 | MWF351 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
29 | 03700386975448 | MWF350S | MWF350S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
30 | 03700386975431 | MWF350 | MWF350 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
31 | 03700386975424 | MWF348S | MWF348S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
32 | 03700386975417 | MWF348 | MWF348 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
33 | 03700386975400 | MWF346S | MWF346S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
34 | 03700386975394 | MWF346 | MWF346 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
35 | 03700386975387 | MWF343S | MWF343S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
36 | 03700386975370 | MWF343 | MWF343 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
37 | 03700386975363 | MWF341S | MWF341S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
38 | 03700386975356 | MWF341 | MWF341 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
39 | 03700386975349 | MWF339S | MWF339S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
40 | 03700386975332 | MWF253S | MWF253S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
41 | 03700386975318 | MWF252S | MWF252S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
42 | 03700386975295 | MWF251S | MWF251S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
43 | 03700386975271 | MWF250S | MWF250S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
44 | 03700386975257 | MWF248S | MWF248S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
45 | 03700386975233 | MWF246S | MWF246S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
46 | 03700386975219 | MWF243S | MWF243S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
47 | 03700386975196 | MWF241S | MWF241S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
48 | 03700386975172 | MWF239S | MWF239S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
49 | 03700386975158 | MWF237S | MWF237S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
50 | 03700386974793 | MWF047 | MWF047 | Punch Template | Tornier Flex | TORNIER |