No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00887517399779 | 6942044 | CoRoent® XLR, 20x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
2 | 00887517399700 | 6941844 | CoRoent® XLR, 18x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
3 | 00887517399335 | 6941644 | CoRoent® XLR, 16x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
4 | 00887517398765 | 6941444 | CoRoent® XLR, 14x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
5 | 00887517398499 | 6941244 | CoRoent® XLR, 12x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
6 | 00887517398420 | 6941044 | CoRoent® XLR, 10x34x24 12° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
7 | 00887517398055 | 6932088 | CoRoent® XLR, 20x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
8 | 00887517397683 | 6931888 | CoRoent® XLR, 18x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
9 | 00887517397256 | 6931688 | CoRoent® XLR, 16x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
10 | 00887517396822 | 6931488 | CoRoent® XLR, 14x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
11 | 00887517396457 | 6931288 | CoRoent® XLR, 12x38x28 15° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
12 | 00887517395641 | 6922088 | CoRoent® XLR, 20x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
13 | 00887517395634 | 6922044 | CoRoent® XLR, 20x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
14 | 00887517395269 | 6921888 | CoRoent® XLR, 18x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
15 | 00887517395252 | 6921844 | CoRoent® XLR, 18x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
16 | 00887517394880 | 6921688 | CoRoent® XLR, 16x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
17 | 00887517394873 | 6921660 | CoRoent® XL Wide, 16x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
18 | 00887517394866 | 6921655 | CoRoent® XL Wide, 16x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
19 | 00887517394859 | 6921650 | CoRoent® XL Wide, 16x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
20 | 00887517394842 | 6921645 | CoRoent® XL Wide, 16x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
21 | 00887517394835 | 6921644 | CoRoent® XLR, 16x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
22 | 00887517394569 | 6921488 | CoRoent® XLR, 14x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
23 | 00887517394552 | 6921460 | CoRoent® XL Wide, 14x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
24 | 00887517394545 | 6921455 | CoRoent® XL Wide, 14x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
25 | 00887517394538 | 6921450 | CoRoent® XL Wide, 14x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
26 | 00887517394521 | 6921445 | CoRoent® XL Wide, 14x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
27 | 00887517394514 | 6921444 | CoRoent® XLR, 14x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
28 | 00887517394149 | 6921288 | CoRoent® XLR, 12x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
29 | 00887517394132 | 6921260 | CoRoent® XL Wide, 12x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
30 | 00887517394125 | 6921255 | CoRoent® XL Wide, 12x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
31 | 00887517394118 | 6921250 | CoRoent® XL Wide, 12x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
32 | 00887517394101 | 6921245 | CoRoent® XL Wide, 12x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
33 | 00887517393791 | 6921244 | CoRoent® XLR, 12x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
34 | 00887517393722 | 6921088 | CoRoent® XLR, 10x38x28 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
35 | 00887517393715 | 6921060 | CoRoent® XL Wide, 10x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
36 | 00887517393708 | 6921055 | CoRoent® XL Wide, 10x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
37 | 00887517393395 | 6921050 | CoRoent® XL Wide, 10x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
38 | 00887517393388 | 6921045 | CoRoent® XL Wide, 10x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
39 | 00887517393371 | 6921044 | CoRoent® XLR, 10x34x24 8° | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
40 | 00887517393333 | 6920860 | CoRoent® XL Wide, 8x22x60mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
41 | 00887517393326 | 6920855 | CoRoent® XL Wide, 8x22x55mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
42 | 00887517393319 | 6920850 | CoRoent® XL Wide, 8x22x50mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
43 | 00887517393302 | 6920845 | CoRoent® XL Wide, 8x22x45mm Lordotic | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
44 | 00887517392961 | 6916860 | CoRoent® XL, 16x18x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
45 | 00887517392954 | 6916855 | CoRoent® XL, 16x18x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
46 | 00887517392947 | 6916850 | CoRoent® XL, 16x18x50mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
47 | 00887517392930 | 6916845 | CoRoent® XL, 16x18x45mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
48 | 00887517392923 | 6916840 | CoRoent® XL, 16x18x40mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
49 | 00887517392916 | 6916260 | CoRoent® XL Wide, 16x22x60mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent | |
50 | 00887517392909 | 6916255 | CoRoent® XL Wide, 16x22x55mm | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | CoRoent |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 07640450869326 | SPE-US 3L 26-N | SPE-US 3L 26-N | SMOOTH HL TRIAL LARGE H26 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
2 | 07640450869319 | SPE-US 3L 24-N | SPE-US 3L 24-N | SMOOTH HL TRIAL LARGE H24 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
3 | 07640450869302 | SPE-US 3L 22-N | SPE-US 3L 22-N | SMOOTH HL TRIAL LARGE H22 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
4 | 07640450869296 | SPE-US 3L 20-N | SPE-US 3L 20-N | SMOOTH HL TRIAL LARGE H20 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
5 | 07640450869289 | SPE-US 2L 25-N | SPE-US 2L 25-N | SMOOTH HL TRIAL LARGE H25 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
6 | 07640450869272 | SPE-US 2L 23-N | SPE-US 2L 23-N | SMOOTH HL TRIAL LARGE H23 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
7 | 07640450869265 | SPE-US 2L 21-N | SPE-US 2L 21-N | SMOOTH HL TRIAL LARGE H21 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
8 | 07640450869258 | SPE-US 2L 19-N | SPE-US 2L 19-N | SMOOTH HL TRIAL LARGE H19 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
9 | 07640450869241 | SPE-US 1L 21-N | SPE-US 1L 21-N | SMOOTH HL TRIAL LARGE H21 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
10 | 07640450869234 | SPE-US 1L 19-N | SPE-US 1L 19-N | SMOOTH HL TRIAL LARGE H19 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
11 | 07640450869227 | SPE-US 1L 17-N | SPE-US 1L 17-N | SMOOTH HL TRIAL LARGE H17 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
12 | 07640450869210 | SPE-US 1L 15-N | SPE-US 1L 15-N | SMOOTH HL TRIAL LARGE H15 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
13 | 07640450869203 | SPE-US 3M 25-N | SPE-US 3M 25-N | SMOOTH HL TRIAL MEDIUM H25 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
14 | 07640450869197 | SPE-US 3M 23-N | SPE-US 3M 23-N | SMOOTH HL TRIAL MEDIUM H23 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
15 | 07640450869180 | SPE-US 3M 21-N | SPE-US 3M 21-N | SMOOTH HL TRIAL MEDIUM H21 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
16 | 07640450869173 | SPE-US 3M 19-N | SPE-US 3M 19-N | SMOOTH HL TRIAL MEDIUM H19 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
17 | 07640450869166 | SPE-US 2M 24-N | SPE-US 2M 24-N | SMOOTH HL TRIAL MEDIUM H24 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
18 | 07640450869159 | SPE-US 2M 22-N | SPE-US 2M 22-N | SMOOTH HL TRIAL MEDIUM H22 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
19 | 07640450869142 | SPE-US 2M 20-N | SPE-US 2M 20-N | SMOOTH HL TRIAL MEDIUM H20 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
20 | 07640450869135 | SPE-US 2M 18-N | SPE-US 2M 18-N | SMOOTH HL TRIAL MEDIUM H18 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
21 | 07640450869128 | SPE-US 1M 20-N | SPE-US 1M 20-N | SMOOTH HL TRIAL MEDIUM H20 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
22 | 07640450869111 | SPE-US 1M 18-N | SPE-US 1M 18-N | SMOOTH HL TRIAL MEDIUM H18 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
23 | 07640450869104 | SPE-US 1M 16-N | SPE-US 1M 16-N | SMOOTH HL TRIAL MEDIUM H16 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
24 | 07640450869098 | SPE-US 1M 14-N | SPE-US 1M 14-N | SMOOTH HL TRIAL MEDIUM H14 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
25 | 07640450869081 | SPE-US 3S 23-N | SPE-US 3S 21-N | SMOOTH HL TRIAL SMALL H23 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
26 | 07640450869074 | SPE-US 3S 21-N | SPE-US 3S 21-N | SMOOTH HL TRIAL SMALL H21 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
27 | 07640450869067 | SPE-US 3S 19-N | SPE-US 3S 19-N | SMOOTH HL TRIAL SMALL H19 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
28 | 07640450869050 | SPE-US 3S 17-N | SPE-US 3S 17-N | SMOOTH HL TRIAL SMALL H17 LORDOSIS 30° | SCARLET® AL-T | SPINEART SA |
29 | 07640450869043 | SPE-US 2S 21-N | SPE-US 2S 21-N | SMOOTH HL TRIAL SMALL H21 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
30 | 07640450869036 | SPE-US 2S 19-N | SPE-US 2S 19-N | SMOOTH HL TRIAL SMALL H19 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
31 | 07640450869029 | SPE-US 2S 17-N | SPE-US 2S 17-N | SMOOTH HL TRIAL SMALL H17 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
32 | 07640450869012 | SPE-US 2S 15-N | SPE-US 2S 15-N | SMOOTH HL TRIAL SMALL H15 LORDOSIS 25° | SCARLET® AL-T | SPINEART SA |
33 | 07640450869005 | SPE-US 1S 19-N | SPE-US 1S 19-N | SMOOTH HL TRIAL SMALL H19 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
34 | 07640450868992 | SPE-US 1S 17-N | SPE-US 1S 17-N | SMOOTH HL TRIAL SMALL H17 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
35 | 07640450868985 | SPE-US 1S 15-N | SPE-US 1S 15-N | SMOOTH HL TRIAL SMALL H15 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
36 | 07640450868978 | SPE-US 1S 13-N | SPE-US 1S 13-N | SMOOTH HL TRIAL SMALL H13 LORDOSIS 20° | SCARLET® AL-T | SPINEART SA |
37 | 07640450866196 | SPE-US 00 92-N | SPE-US 00 92-N | Windowed Cage and Plate Holder | JULIET® Ti LL | SPINEART SA |
38 | 07640450863317 | DYN-IT 01 03-N | DYN-IT 01 03-N | IMPLANT HOLDER HANDLE (JULIET ® TL) | JULIET TL Instruments | SPINEART SA |
39 | 07640450863300 | DYN-IT 01 02-N | DYN-IT 01 02-N | IMPLANT HOLDER TUBE (JULIET ® TL) | JULIET TL Instruments | SPINEART SA |
40 | 07640450863294 | DYN-IT 01 01-N | DYN-IT 01 01-N | IMPLANT HOLDER SHAFT (JULIET ® TL) | JULIET TL Instruments | SPINEART SA |
41 | 07640450862624 | SPE-US S5 18-N | SPE-US S5 18-N | SMOOTH TRIAL Small | SCARLET® AL-T | SPINEART SA |
42 | 07640450862617 | SPE-US S0 18-N | SPE-US S0 18-N | SMOOTH TRIAL Small | SCARLET® AL-T | SPINEART SA |
43 | 07640450862600 | SPE-US M5 18-N | SPE-US M5 18-N | SMOOTH TRIAL Médium | SCARLET® AL-T | SPINEART SA |
44 | 07640450862594 | SPE-US M0 18-N | SPE-US L5 18-N | SMOOTH TRIAL Médium | SCARLET® AL-T | SPINEART SA |
45 | 07640450862587 | SPE-US L5 18-N | SPE-US L5 18-N | SMOOTH TRIAL Large | SCARLET® AL-T | SPINEART SA |
46 | 07640375235169 | SPE-US 01 28-N | SPE-US 01 28-N | IMPLANT HOLDER-L | SCARLET® AL-T | SPINEART SA |
47 | 07640375235152 | SPE-US 01 27-N | SPE-US 01 27-N | IMPLANT HOLDER-SM | SCARLET® AL-T | SPINEART SA |
48 | 07640375235145 | SPE-US 01 25-N | SPE-US 01 25-N | OLIF IMPLANT HOLDER-L | SCARLET® AL-T | SPINEART SA |
49 | 07640375235138 | SPE-US 01 24-N | SPE-US 01 24-N | OLIF IMPLANT HOLDER-SM | SCARLET® AL-T | SPINEART SA |
50 | 07640375235107 | SPE-US 01 18-N | SPE-US 01 18-N | THREADED U-JOINT | SCARLET® AL-T | SPINEART SA |