| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 00880304547643 | 32-422777 | 32-422777 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford® Uni Knee System | |
| 2 | 00880304525658 | 32-422760 | 32-422760 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 3 | 00880304525641 | 32-422812 | 32-422812 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 4 | 00880304525634 | 32-422811 | 32-422811 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 5 | 00880304525542 | 32-422802 | 32-422802 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 6 | 00880304525535 | 32-422806 | 32-422806 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 7 | 00880304525467 | 32-422803 | 32-422803 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 8 | 00880304525450 | 32-423231 | 32-423231 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 9 | 00880304525443 | 32-422771 | 32-422771 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 10 | 00880304525436 | 32-422805 | 32-422805 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 11 | 00880304525429 | 32-423223 | 32-423223 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 12 | 00880304525412 | 32-422804 | 32-422804 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 13 | 00880304525382 | 32-422801 | 32-422801 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 14 | 00880304509696 | 32-422977 | 32-422977 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
| 15 | 00880304504714 | 32-422845 | 32-422845 | HTW | BIT, DRILL | 1 | Oxford Uni Knee System | |
| 16 | 00880304504707 | 32-423228 | 32-423228 | HTW | BIT, DRILL | 1 | Oxford® Uni Knee System | |
| 17 | 00880304007581 | 595250 | 595250 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | MICROPLASTY HIP | |
| 18 | 05019279999439 | 154373 | 154373 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 19 | 05019279999422 | 154372 | 154372 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 20 | 05019279999415 | 154371 | 154371 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 21 | 05019279999453 | 154375 | 154375 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 22 | 05019279999446 | 154374 | 154374 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 23 | 05019279999491 | 154379 | 154379 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 24 | 05019279999484 | 154378 | 154378 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 25 | 05019279999477 | 154377 | 154377 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 26 | 05019279999460 | 154376 | 154376 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
| 27 | 05019279998319 | 110028563 | 110028563 | GAD | RETRACTOR | 1 | ASI INSTRUMENTSCOBRA STYLE RETRACTOR | |
| 28 | 05019279924271 | 31-500960 | 31-500960 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 29 | 05019279924257 | 31-500958 | 31-500958 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 30 | 05019279924233 | 31-500956 | 31-500956 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 31 | 05019279924219 | 31-500954 | 31-500954 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 32 | 05019279924196 | 31-500952 | 31-500952 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 33 | 05019279924172 | 31-500950 | 31-500950 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 34 | 05019279924158 | 31-500948 | 31-500948 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 35 | 05019279924134 | 31-500946 | 31-500946 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 36 | 05019279924110 | 31-500944 | 31-500944 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 37 | 05019279924097 | 31-500942 | 31-500942 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 38 | 05019279924073 | 31-500940 | 31-500940 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 39 | 05019279924059 | 31-500938 | 31-500938 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
| 40 | 05019279924011 | 31-500760 | 31-500760 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 41 | 05019279924004 | 31-500758 | 31-500758 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 42 | 05019279923991 | 31-500756 | 31-500756 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 43 | 05019279923984 | 31-500754 | 31-500754 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 44 | 05019279923977 | 31-500752 | 31-500752 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 45 | 05019279923960 | 31-500750 | 31-500750 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 46 | 05019279923953 | 31-500748 | 31-500748 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 47 | 05019279923946 | 31-500746 | 31-500746 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 48 | 05019279923939 | 31-500744 | 31-500744 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 49 | 05019279923922 | 31-500742 | 31-500742 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
| 50 | 05019279923915 | 31-500740 | 31-500740 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00889024041172 | 2241-01-01 | M/DN® | ZIMMER, INC. | ||
| 2 | 00889024034969 | 1179-09 | 00-1179-009-00 | NA | ZIMMER, INC. | |
| 3 | 00889024036420 | 1193-23 | Versa-Fx® | ZIMMER, INC. | ||
| 4 | 00889024036413 | 1193-22 | Versa-Fx® | ZIMMER, INC. | ||
| 5 | 00889024034808 | 1179-07 | 00-1179-007-00 | NA | ZIMMER, INC. | |
| 6 | 00889024034457 | 1161-07 | 00-1161-007-00 | NA | ZIMMER, INC. | |
| 7 | 00889024010321 | 07.02099.003 | 07.02099.003 | Vitality® | ZIMMER SPINE, INC. | |
| 8 | 00889024010314 | 07.02099.002 | 07.02099.002 | Vitality® | ZIMMER SPINE, INC. | |
| 9 | 00889024010307 | 07.02099.001 | 07.02099.001 | Vitality® | ZIMMER SPINE, INC. | |
| 10 | 00888912545402 | 800-88-113 | EMPOWR PS KNEE X-RAY TEMPLATE, NP TIBIA | DJO SURGICAL | ENCORE MEDICAL, L.P. | |
| 11 | 00888912150941 | 804-88-117 | TURON SHOULDER SYSTEM, X-RAY TEMPLATE, ASSEMBLY | DJO SURGICAL | DJO, LLC | |
| 12 | 00888912142076 | 800-88-106 | MOVATION X-RAY TEMPLATES | DJO SURGICAL | ENCORE MEDICAL, L.P. | |
| 13 | 00888912142052 | 800-88-102 | 3D KNEE X-RAY TEMPLATES ASSEMBLY | DJO SURGICAL | ENCORE MEDICAL, L.P. | |
| 14 | 00888912105217 | 803-88-001 | LINEAR LATERAL XRAY TEMPLATES | DJO SURGICAL | ENCORE MEDICAL, L.P. | |
| 15 | 00888912105200 | 803-88-000 | LINEAR STANDARD XRAY TEMPLATES | DJO SURGICAL | ENCORE MEDICAL, L.P. | |
| 16 | 00888867236929 | AR-4084S-14 | AR-4084S-14 | Dilator / TrialSmall-14 | Arthrex® | ARTHREX, INC. |
| 17 | 00888867220546 | AR-8942T-1808 | AR-8942T-1808 | Evans Wedge Trial, 18x18x8 mm | Arthrex® | ARTHREX, INC. |
| 18 | 00888912092937 | 803-05-130 | TRL.ACETABULAR SHELL 40MM FMP | DJO SURGICAL | DJO, LLC | |
| 19 | 00888867350922 | AR-9236-04AG-25L | AR-9236-04AG-25L | AUGMENTED VAULTLOCK TRIAL, X-LARGE 25L | Arthrex® | ARTHREX, INC. |
| 20 | 00888867350915 | AR-9236-04AG-25R | AR-9236-04AG-25R | AUGMENTED VAULTLOCK TRIAL, X-LARGE 25R | Arthrex® | ARTHREX, INC. |
| 21 | 00888867350908 | AR-9236-04AG-15L | AR-9236-04AG-15L | AUGMENTED VAULTLOCK TRIAL, X-LARGE 15L | Arthrex® | ARTHREX, INC. |
| 22 | 00888867350892 | AR-9236-04AG-15R | AR-9236-04AG-15R | AUGMENTED VAULTLOCK TRIAL, X-LARGE 15R | Arthrex® | ARTHREX, INC. |
| 23 | 00888867350885 | AR-9236-03AG-25L | AR-9236-03AG-25L | AUGMENTED VAULTLOCK TRIAL, LARGE 25L | Arthrex® | ARTHREX, INC. |
| 24 | 00888867350878 | AR-9236-03AG-25R | AR-9236-03AG-25R | AUGMENTED VAULTLOCK TRIAL, LARGE 25R | Arthrex® | ARTHREX, INC. |
| 25 | 00888867350861 | AR-9236-03AG-15L | AR-9236-03AG-15L | AUGMENTED VAULTLOCK TRIAL, LARGE 15L | Arthrex® | ARTHREX, INC. |
| 26 | 00888867350854 | AR-9236-03AG-15R | AR-9236-03AG-15R | AUGMENTED VAULTLOCK TRIAL, LARGE 15R | Arthrex® | ARTHREX, INC. |
| 27 | 00888867350847 | AR-9236-02AG-25L | AR-9236-02AG-25L | AUGMENTED VAULTLOCK TRIAL, MEDIUM 25L | Arthrex® | ARTHREX, INC. |
| 28 | 00888867350830 | AR-9236-02AG-25R | AR-9236-02AG-25R | AUGMENTED VAULTLOCK TRIAL, MEDIUM 25R | Arthrex® | ARTHREX, INC. |
| 29 | 00888867350823 | AR-9236-02AG-15L | AR-9236-02AG-15L | AUGMENTED VAULTLOCK TRIAL, MEDIUM 15L | Arthrex® | ARTHREX, INC. |
| 30 | 00888867350816 | AR-9236-02AG-15R | AR-9236-02AG-15R | AUGMENTED VAULTLOCK TRIAL, MEDIUM 15R | Arthrex® | ARTHREX, INC. |
| 31 | 00888867350632 | AR-9236-01AG-25L | AR-9236-01AG-25L | AUGMENTED VAULTLOCK TRIAL, SMALL 25L | Arthrex® | ARTHREX, INC. |
| 32 | 00888867350601 | AR-9236-01AG-25R | AR-9236-01AG-25R | AUGMENTED VAULTLOCK TRIAL, SMALL 25R | Arthrex® | ARTHREX, INC. |
| 33 | 00888867350595 | AR-9236-01AG-15L | AR-9236-01AG-15L | AUGMENTED VAULTLOCK TRIAL, SMALL 15L | Arthrex® | ARTHREX, INC. |
| 34 | 00888867350588 | AR-9236-01AG-15R | AR-9236-01AG-15R | AUGMENTED VAULTLOCK TRIAL, SMALL 15R | Arthrex® | ARTHREX, INC. |
| 35 | 00888867350564 | AR-9236-04AG-25BP | AR-9236-04AG-25BP | AVL BONE PREP TRIAL, XL 25 | Arthrex® | ARTHREX, INC. |
| 36 | 00888867350557 | AR-9236-04AG-15BP | AR-9236-04AG-15BP | AVL BONE PREP TRIAL, XL 15 | Arthrex® | ARTHREX, INC. |
| 37 | 00888867350540 | AR-9236-03AG-25BP | AR-9236-03AG-25BP | AVL BONE PREP TRIAL, L 25 | Arthrex® | ARTHREX, INC. |
| 38 | 00888867350533 | AR-9236-03AG-15BP | AR-9236-03AG-15BP | AVL BONE PREP TRIAL, L 15 | Arthrex® | ARTHREX, INC. |
| 39 | 00888867350526 | AR-9236-02AG-25BP | AR-9236-02AG-25BP | AVL BONE PREP TRIAL, M 25 | Arthrex® | ARTHREX, INC. |
| 40 | 00888867350519 | AR-9236-02AG-15BP | AR-9236-02AG-15BP | AVL BONE PREP TRIAL, M 15 | Arthrex® | ARTHREX, INC. |
| 41 | 00888867350502 | AR-9236-01AG-25BP | AR-9236-01AG-25BP | AVL BONE PREP TRIAL, S 25 | Arthrex® | ARTHREX, INC. |
| 42 | 00888867350496 | AR-9236-01AG-15BP | AR-9236-01AG-15BP | AVL BONE PREP TRIAL, S 15 | Arthrex® | ARTHREX, INC. |
| 43 | 00888867347953 | AR-611-39 | AR-611-39 | iBal UKA, Tibial D-Ring Trial, Size 6 | Arthrex® | ARTHREX, INC. |
| 44 | 00888867347946 | AR-611-38 | AR-611-38 | iBal UKA, Tibial D-Ring Trial, Size 5 | Arthrex® | ARTHREX, INC. |
| 45 | 00888867347939 | AR-611-37 | AR-611-37 | iBal UKA, Tibial D-Ring Trial, Size 4 | Arthrex® | ARTHREX, INC. |
| 46 | 00888867347922 | AR-611-36 | AR-611-36 | iBal UKA, Tibial D-Ring Trial, Size 3 | Arthrex® | ARTHREX, INC. |
| 47 | 00888867347915 | AR-611-35 | AR-611-35 | iBal UKA, Tibial D-Ring Trial, Size 2 | Arthrex® | ARTHREX, INC. |
| 48 | 00888867347908 | AR-611-34 | AR-611-34 | iBal UKA, Tibial D-Ring Trial, Size 1 | Arthrex® | ARTHREX, INC. |
| 49 | 00888867343832 | AR-9594-2820 | AR-9594-2820 | 28MM BASEPLATE, 20° FULL AUGMENT TRIAL | Arthrex® | ARTHREX, INC. |
| 50 | 00888867343825 | AR-9594-2810 | AR-9594-2810 | 28MM BASEPLATE, 10° FULL AUGMENT TRIAL | Arthrex® | ARTHREX, INC. |