| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00817577023802 | A | 2000-7029 | Syndesmosis Plate | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 2 | 00817577023796 | A | 2000-7028 | Straight Plate Contoured - 14 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 3 | 00817577024823 | A | 2100-7001 | Medial Hook Plate Drill Guide | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 4 | 00817577024816 | A | 2100-7000 | Medial Hook Plate Impactor | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 5 | 00817577024342 | A | 2001-4060 | 4.0mm Non-Locking Screw x 60mm | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 6 | 00817577024311 | A | 2001-4055 | 4.0mm Non-Locking Screw x 55mm | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 7 | 00817577024281 | A | 2001-4050 | 4.0mm Non-Locking Screw x 50mm | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 8 | 00817577024250 | A | 2001-4045 | 4.0mm Non-Locking Screw x 45mm | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 9 | 00817577023789 | A | 2000-7027 | Straight Plate Contoured - 12 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 10 | 00817577023772 | A | 2000-7026 | Straight Plate Contoured - 10 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 11 | 00817577023765 | A | 2000-7025 | Straight Plate Contoured - 8 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 12 | 00817577023758 | A | 2000-7024 | Straight Plate Contoured - 6 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 13 | 00817577023741 | A | 2000-7023 | Universal Recon Plate - 17 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 14 | 00817577023734 | A | 2000-7022 | Universal Recon Plate - 15 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 15 | 00817577023727 | A | 2000-7021 | Universal Recon Plate - 13 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 16 | 00817577023710 | A | 2000-7020 | Universal Recon Plate - 11 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 17 | 00817577023703 | A | 2000-7019 | Universal Recon Plate - 9 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 18 | 00817577023697 | A | 2000-7018 | Straight Plate - 14 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 19 | 00817577023680 | A | 2000-7017 | Straight Plate - 12 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 20 | 00817577023673 | A | 2000-7016 | Straight Plate - 10 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 21 | 00817577023666 | A | 2000-7015 | Straight Plate - 8 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 22 | 00817577023659 | A | 2000-7014 | Straight Plate - 6 Hole | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 23 | 00817577023642 | A | 2000-7013 | Posterior Plate - Long | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 24 | 00817577023635 | A | 2000-7012 | Posterior Plate - Std | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 25 | 00817577023628 | B | 2000-7011 | Left Lateral Fibula Plate - Xlong | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 26 | 00817577023611 | B | 2000-7010 | Left Lateral Fibula Plate - Long | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 27 | 00817577023604 | B | 2000-7009 | Left Lateral Fibula Plate - STD | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 28 | 00817577023598 | B | 2000-7008 | Right Lateral Fibula Plate - XLong | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 29 | 00817577023581 | B | 2000-7007 | Right Lateral Fibula Plate - Long | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 30 | 00817577023574 | B | 2000-7006 | Right Lateral Fibula Plate - Std | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 31 | 00817577023567 | B | 2000-7005 | Universal Lateral Fibula Plate - XLong | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 32 | 00817577023550 | B | 2000-7004 | Universal Lateral Fibula Plate - Long | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM |
| 33 | 00817577023543 | B | 2000-7003 | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM | |
| 34 | 00817577023536 | A | 2000-7002 | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM | |
| 35 | 00817577023529 | A | 2000-7001 | HRS | Plate, Fixation, Bone | 2 | EPIC FRACTURE PLATE SYSTEM | |
| 36 | 00817577023512 | 1100-0005 | 1100-0005 | RATCHET HANDLE, LARGE | HXX | SCREWDRIVER | 1 | NA |
| 37 | 00817577023505 | 1100-0004 | 1100-0004 | RATCHET HANDLE, SMALL | HXX | SCREWDRIVER | 1 | NA |
| 38 | 00817577023208 | 4100-0001 | 4100-0001 | SNAP-OFF DRIVER | HWC | Screw, fixation, bone | 2 | NA |
| 39 | 00817577023130 | 2100-2700 | 2100-2700 | 2.7MM SOLID DRILL BIT | HRS | Plate, fixation, bone | 2 | NA |
| 40 | 00817577022898 | 2100-2009 | 2100-2009 | SPREADER (OPENING WEDGE) | LXH | Orthopedic manual surgical instrument | 1 | NA |
| 41 | 00817577022881 | 2100-2027 | 2100-2027 | 2.0/2.7DOUBLEENDE DRILLGUIDE | HRS | Plate, fixation, bone | 2 | NA |
| 42 | 00817577022874 | 2100-2000 | 2100-2000 | 2.0MM SOLID DRILL BIT | HRS | Plate, fixation, bone | 2 | NA |
| 43 | 00817577022867 | 2100-1023 | 2100-1023 | 22MM CONE REAMER | HTO | REAMER | 1 | NA |
| 44 | 00817577022850 | 2100-1022 | 2100-1022 | 22MM CUP REAMER | HTO | REAMER | 1 | NA |
| 45 | 00817577022843 | 2100-1021 | 2100-1021 | 20MM CONE REAMER | HTO | REAMER | 1 | NA |
| 46 | 00817577022836 | 2100-1020 | 2100-1020 | 20MM CUP REAMER | HTO | REAMER | 1 | NA |
| 47 | 00817577022829 | 2100-1019 | 2100-1019 | 18MM CONE REAMER | HTO | REAMER | 1 | NA |
| 48 | 00817577022812 | 2100-1018 | 2100-1018 | 18MM CUP REAMER | HTO | REAMER | 1 | NA |
| 49 | 00817577022805 | 2100-1017 | 2100-1017 | 16MM CONE REAMER | HTO | REAMER | 1 | NA |
| 50 | 00817577022799 | 2100-1016 | 2100-1016 | 16MM CUP REAMER | HTO | REAMER | 1 | NA |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 08031497002903 | SPK03Z1 | InterSpace Knee Trial XL is intended to be used for the selection of the right s InterSpace Knee Trial XL is intended to be used for the selection of the right size of InterSpace Knee XL to be implanted. | InterSpace Knee Trial XL | TECRES SPA | |
| 2 | 08031497002897 | SPK90Z2 | InterSpace Knee ATS Trial Kit is intended to be used for the selection of the ri InterSpace Knee ATS Trial Kit is intended to be used for the selection of the right size and thickness of the InterSpace Knee ATS to be implanted. | InterSpace Knee ATS Trial Kit | TECRES SPA | |
| 3 | 08031497002880 | SPC91Z1 | InterSpace Hip Trial XL is intended to be used for the selection of the right si InterSpace Hip Trial XL is intended to be used for the selection of the right size of InterSpace Hip XL to be implanted. | InterSpace Hip Trial XL | TECRES SPA | |
| 4 | 08031497002873 | SPC90Z1 | InterSpace Hip Trial is intended to be used for the selection of the right size InterSpace Hip Trial is intended to be used for the selection of the right size of InterSpace Hip to be implanted. | InterSpace Hip Trial | TECRES SPA | |
| 5 | 08031497002866 | SPC90Z3 | InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of InterSpace Tapered Wedge Stem Trial is intended to be used for the selection of the right size of InterSpace Tapered Wedge Stem to be implanted. | InterSpace Tapered Wedge Stem Trial | TECRES SPA | |
| 6 | 08031497002347 | SPK90Z1 | InterSpace Knee Trial is intended to be used for the selection of the right size InterSpace Knee Trial is intended to be used for the selection of the right size of InterSpace Knee to be implanted. | InterSpace Knee Trial | TECRES SPA | |
| 7 | 08031497002323 | SPC91Z3 | InterSpace Tapered Wedge Stem Trial XL is intended to be used for the selection InterSpace Tapered Wedge Stem Trial XL is intended to be used for the selection of the right size of InterSpace Tapered Wedge Stem XL to be implanted. | InterSpace Tapered Wedge Stem Trial XL | TECRES SPA | |
| 8 | 08031497002040 | SPS90Z1 | InterSpace Shoulder Trial is intended to be used for the selection of the right InterSpace Shoulder Trial is intended to be used for the selection of the right size of InterSpace Shoulder to be implanted. | InterSpace Shoulder Trial | TECRES SPA | |
| 9 | 07640450865571 | SPE-US 00 88-N | SPE-US 00 88-N | LATERAL RASP TRIAL 21MM H14 | JULIET ® LL | SPINEART SA |
| 10 | 07640450865564 | SPE-US 00 87-N | SPE-US 00 87-N | LATERAL RASP TRIAL 21MM H12 | JULIET ® LL | SPINEART SA |
| 11 | 07640450865557 | SPE-US 00 86-N | SPE-US 00 86-N | LATERAL RASP TRIAL 21MM H10 | JULIET ® LL | SPINEART SA |
| 12 | 07640450865540 | SPE-US 00 85-N | SPE-US 00 85-N | LATERAL RASP TRIAL 21MM H08 | JULIET ® LL | SPINEART SA |
| 13 | 07640450865533 | SPE-US 00 84-N | SPE-US 00 84-N | LATERAL RASP TRIAL 17MM H14 | JULIET ® LL | SPINEART SA |
| 14 | 07640450865526 | SPE-US 00 83-N | SPE-US 00 83-N | LATERAL RASP TRIAL 17MM H12 | JULIET ® LL | SPINEART SA |
| 15 | 07640450865519 | SPE-US 00 82-N | SPE-US 00 82-N | LATERAL RASP TRIAL 17MM H10 | JULIET ® LL | SPINEART SA |
| 16 | 07640450865502 | SPE-US 00 81-N | SPE-US 00 81-N | LATERAL RASP TRIAL 17MM H08 | JULIET ® LL | SPINEART SA |
| 17 | 07640178983984 | JUT-IN 05 13-N | JUT-IN 05 13-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 18 | 07640178983977 | JUT-IN 05 12-N | JUT-IN 05 12-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 19 | 07640178983960 | JUT-IN 05 11-N | JUT-IN 05 11-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 20 | 07640178983953 | JUT-IN 05 10-N | JUT-IN 05 10-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 21 | 07640178983946 | JUT-IN 05 09-N | JUT-IN 05 09-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 22 | 07640178983939 | JUT-IN 05 08-N | JUT-IN 05 08-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 23 | 07640178983922 | JUT-IN 06 16-N | JUT-IN 06 16-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 24 | 07640178983915 | JUT-IN 06 15-N | JUT-IN 06 15-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 25 | 07640178983908 | JUT-IN 06 14-N | JUT-IN 06 14-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 26 | 07640178983892 | JUT-IN 06 13-N | JUT-IN 06 13-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 27 | 07640178983885 | JUT-IN 06 12-N | JUT-IN 06 12-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 28 | 07640185341234 | SPE-IN 01 53-N | SPE-IN 01 53-N | Rasp Trial 14 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 29 | 07640185341227 | SPE-IN 01 52-N | SPE-IN 01 52-N | Rasp Trial 12 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 30 | 07640185341210 | SPE-IN 01 51-N | SPE-IN 01 51-N | Rasp Trial 10 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 31 | 07640185341203 | SPE-IN 01 50-N | SPE-IN 01 50-N | Rasp Trial 08 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 32 | 07640185341197 | SPE-IN 01 49-N | SPE-IN 01 49-N | Barrel – 12 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 33 | 07640185341180 | SPE-IN 01 48-N | SPE-IN 01 48-N | Barrel – 12 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 34 | 07640185341173 | SPE-IN 01 47-N | SPE-IN 01 47-N | Barrel – 10 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 35 | 07640185341166 | SPE-IN 01 46-N | SPE-IN 01 46-N | Barrel – 08 | ROMEO 2 PAD INSTRUMENTATION | SPINEART SA |
| 36 | 07640178988842 | SPE-US 00 31-N | SPE-US 00 31-N | SCREW BLOCK | ROMEO 2 INSTRUMENTATION | SPINEART SA |
| 37 | 07640178983878 | JUT-IN 06 11-N | JUT-IN 06 11-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 38 | 07640178983991 | JUT-IN 05 14-N | JUT-IN 05 14-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 39 | 07640178984028 | MIS-IN 51 00-N | MIS-IN 51 00-N | INCISION TEMPLATE | ROMEO 2 INSTRUMENTATION | SPINEART SA |
| 40 | 07640178984011 | JUT-IN 05 16-N | JUT-IN 05 16-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 41 | 07640178984004 | JUT-IN 05 15-N | JUT-IN 05 15-N | TRIAL IMPLANT Ti TL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 42 | 07640178983861 | JUT-IN 06 10-N | JUT-IN 06 10-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 43 | 07640178983854 | JUT-IN 06 09-N | JUT-IN 06 09-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 44 | 07640178983847 | JUT-IN 06 08-N | JUT-IN 06 08-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 45 | 07640178983830 | JUT-IN 06 07-N | JUT-IN 06 07-N | TRIAL IMPLANT Ti PO/OL SMOOTH SMALL WIDTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 46 | 07640178983823 | JUT-IN 04 16-N | JUT-IN 04 16-N | TRIAL IMPLANT Ti PO/OL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 47 | 07640178983816 | JUT-IN 04 15-N | JUT-IN 04 15-N | TRIAL IMPLANT Ti PO/OL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 48 | 07640178983809 | JUT-IN 04 14-N | JUT-IN 04 14-N | TRIAL IMPLANT Ti PO/OL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 49 | 07640178983793 | JUT-IN 04 13-N | JUT-IN 04 13-N | TRIAL IMPLANT Ti PO/OL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |
| 50 | 07640178983786 | JUT-IN 04 12-N | JUT-IN 04 12-N | TRIAL IMPLANT Ti PO/OL SMOOTH | JULIET ® INSTRUMENTATION | SPINEART SA |