| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | M528G00003000 | G000-0300 | G000-0300 | Disposable Reamer 15mm, Glenoid | LXH | Orthopedic Manual Surgical Instrument | 1 | Glenoid GRS |
| 2 | M5288W950016W0 | 8W95-0016-W | 8W95-0016-W | Taper Post, 7.5mm Dia, Capitate, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 3 | M5288W153523W0 | 8W15-3523-W | 8W15-3523-W | 15mm Capitate Component, 35mm x 23mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 4 | M5288W153517W0 | 8W15-3517-W | 8W15-3517-W | 15mm Capitate Component, 35mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 5 | M5288W152223W0 | 8W15-2223-W | 8W15-2223-W | 15mm Capitate Component, 22mm x 23mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 6 | M5288W152217W0 | 8W15-2217-W | 8W15-2217-W | 15mm Capitate Component, 22mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 7 | M5288W123517W0 | 8W12-3517-W | 8W12-3517-W | 12mm Capitate Component, 35mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 8 | M5288W122217W0 | 8W12-2217-W | 8W12-2217-W | 12mm Capitate Component, 22mm x 17mm, Wrist, CE | KWN | Prosthesis, Wrist, Carpal Lunate | 2 | WristMotion® Wrist Hemiarthroplasty System |
| 9 | M528P2051045W0 | P205-1045-W | P205-1045-W | Patella Comp, 20mm, 1.0x4.5mm, Anatomic CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 10 | M528PWR21155W0 | PWR2-1155-W | PWR2-1155-W | Femoral Component, Right, 11.5mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 11 | M528PWR21155A0 | PWR2-1155-A | PWR2-1155-A | Femoral Component, Right, 11.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 12 | M528PWR21005W0 | PWR2-1005-W | PWR2-1005-W | Femoral Component, Right, 10.0mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 13 | M528PWR21005A0 | PWR2-1005-A | PWR2-1005-A | Femoral Component, Right, 10.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 14 | M528PWR20855W0 | PWR2-0855-W | PWR2-0855-W | Femoral Component, Right, 8.5mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 15 | M528PWR20855A0 | PWR2-0855-A | PWR2-0855-A | Femoral Component, Right, 8.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 16 | M528PWR20705W0 | PWR2-0705-W | PWR2-0705-W | Femoral Component, Right, 7.0mm Offset, Kahuna,CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 17 | M528PWR20705A0 | PWR2-0705-A | PWR2-0705-A | Femoral Component, Right, 7.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 18 | M528PWL21155W0 | PWL2-1155-W | PWL2-1155-W | Femoral Component, Left, 11.5 mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 19 | M528PWL21155A0 | PWL2-1155-A | PWL2-1155-A | Femoral Component, Left, 11.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 20 | M528PWL21005W0 | PWL2-1005-W | PWL2-1005-W | Femoral Component, Left, 10.0mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 21 | M528PWL21005A0 | PWL2-1005-A | PWL2-1005-A | Femoral Component, Left, 10.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 22 | M528PWL20855W0 | PWL2-0855-W | PWL2-0855-W | Femoral Component, Left, 8.5mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 23 | M528PWL20855A0 | PWL2-0855-A | PWL2-0855-A | Femoral Component, Left, 8.5 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 24 | M528PWL20705W0 | PWL2-0705-W | PWL2-0705-W | Femoral Component, Left, 7.0mm Offset, Kahuna, CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 25 | M528PWL20705A0 | PWL2-0705-A | PWL2-0705-A | Femoral Component, Left, 7.0 mm Offset, Kahuna | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | WaveKahuna™ |
| 26 | M528P2060045W0 | P206-0045-W | P206-0045-W | Patella Comp, 20mm x 4.5mm, Button CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 27 | M528P2060045A0 | P206-0045-A | P206-0045-A | Patella Comp, 20mm x 4.5mm, Button | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 28 | M528P2060040W0 | P206-0040-W | P206-0040-W | Patella Comp, 20mm x 4.0 mm, Button CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 29 | M528P2060040A0 | P206-0040-A | P206-0040-A | Patella Comp, 20mm x 4.0 mm, Button | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 30 | M528P2060035W0 | P206-0035-W | P206-0035-W | Patella Comp, Button, 20mm, 3.5mm x 3.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 31 | M528P2060035A0 | P206-0035-A | P206-0035-A | Patella Comp, Button, 20mm, 3.5mm x 3.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 32 | M528P2060030W0 | P206-0030-W | P206-0030-W | Patella Comp, Button, 20mm, 3.0mm x 3.0mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 33 | M528P2060030A0 | P206-0030-A | P206-0030-A | Patella Comp, Button, 20mm, 3.0mm x 3.0mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 34 | M528P2060025W0 | P206-0025-W | P206-0025-W | Patella Comp, Button, 20mm, 2.5mm x 2.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 35 | M528P2060025A0 | P206-0025-A | P206-0025-A | Patella Comp, Button, 20mm, 2.5mm x 2.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 36 | M528P2051045A0 | P205-1045-A | P205-1045-A | Patella Comp, 20mm, 1.0x4.5mm, Anatomic | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 37 | M528P2051040W0 | P205-1040-W | P205-1040-W | Patella Comp, 20mm, 1.0x4.0mm, Anatomic CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 38 | M528P2051040A0 | P205-1040-A | P205-1040-A | Patella Comp, 20mm, 1.0x4.0mm, Anatomic | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 39 | M528P2051035W0 | P205-1035-W | P205-1035-W | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 40 | M528P2051035A0 | P205-1035-A | P205-1035-A | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 41 | M528P2051030W0 | P205-1030-W | P205-1030-W | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.0mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 42 | M528P2051030A0 | P205-1030-A | P205-1030-A | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 3.0mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 43 | M528P2051025W0 | P205-1025-W | P205-1025-W | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 2.5mm CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 44 | M528P2051025A0 | P205-1025-A | P205-1025-A | Patella-Femoral, Comp, Anatomic, 20mm, 1.0mm x 2.5mm | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 45 | M528P2023530W0 | P202-3530-W | P202-3530-W | Patello-Femoral, Fem Comp, 3.5x3.0 CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 46 | M528P2023530A0 | P202-3530-A | P202-3530-A | Patello-Femoral, Fem Comp, 3.5x3.0 | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 47 | M528P2023525W0 | P202-3525-W | P202-3525-W | Patello-Femoral, Fem Comp, 3.5x2.5 CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 48 | M528P2023525A0 | P202-3525-A | P202-3525-A | Patello-Femoral, Fem Comp, 3.5x2.5 | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 49 | M528P2023520W0 | P202-3520-W | P202-3520-W | Patello-Femoral, Fem Comp, 3.5x2.0 CE | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| 50 | M528P2023520A0 | P202-3520-A | P202-3520-A | Patello-Femoral, Fem Comp, 3.5x2.0 | KRR | Prosthesis, Knee, Patello/Femoral, Semi-Constrained, Cemented, Metal/Polymer | 2 | HemiCAP® |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 28031497000408 | SPS0121 | Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Shoulder is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion, etc.). | InterSpace Shoulder | TECRES SPA | |
| 2 | 28031497000408 | SPS0121 | Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Shoulder is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion, etc.). | InterSpace Shoulder | TECRES SPA | |
| 3 | 28031497000392 | SPS0021 | Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Shoulder is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion, etc.). | InterSpace Shoulder | TECRES SPA | |
| 4 | 28031497000392 | SPS0021 | Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fu Temporary shoulder spacer with gentamicin. InterSpace Shoulder is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement coated onto a stainless steel reinforcing structure. The device is sterile and single-use.InterSpace Shoulder is indicated for temporary use (maximum of 180 days) as a shoulder replacement (SR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. The head and stem are inserted into the glenoideal cavity and the humeral medullary canal, respectively, following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Shoulder is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion, etc.). | InterSpace Shoulder | TECRES SPA | |
| 5 | 10889024287898 | 01.04255.000 | 01.04255.000 | Anatomical Shoulder™ Bigliani/Flatow® | ZIMMER GMBH | |
| 6 | 10889024287898 | 01.04255.000 | 01.04255.000 | Anatomical Shoulder™ Bigliani/Flatow® | ZIMMER GMBH | |
| 7 | 10886982241658 | 5624-8/20XL | 5624820XL | COCR HUMERAL STEM CEMENTED SIZE 8/200MM XLONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 8 | 10886982241641 | 5624-8/16L | 5624816L | COCR HUMERAL STEM CEMENTED SIZE 8/160MM LONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 9 | 10886982241634 | 5624-8/12 | 5624812 | COCR HUMERAL STEM CEMENTED SIZE 8/120MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 10 | 10886982241627 | 5624-6/19XL | 5624619XL | COCR HUMERAL STEM CEMENTED SIZE 6/195MM XLONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 11 | 10886982241610 | 5624-6/15L | 5624615L | COCR HUMERAL STEM CEMENTED SIZE 6/155MM LONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 12 | 10886982241603 | 5624-6/11 | 5624611 | COCR HUMERAL STEM CEMENTED SIZE 6/115MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 13 | 10886982241597 | 5624-14/21XL | 56241421XL | COCR HUMERAL STEM CEMENTED SIZE 14/215MM XLONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 14 | 10886982241580 | 5624-14/17L | 56241417L | COCR HUMERAL STEM CEMENTED SIZE 14/175MM LONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 15 | 10886982241573 | 5624-14/13 | 56241413 | COCR HUMERAL STEM CEMENTED SIZE 14/135MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 16 | 10886982241566 | 5624-12/21XL | 56241221XL | COCR HUMERAL STEM CEMENTED SIZE 12/210MM XLONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 17 | 10886982241559 | 5624-12/17L | 56241217L | COCR HUMERAL STEM CEMENTED SIZE 12/170MM LONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 18 | 10886982241542 | 5624-12/13 | 56241213 | COCR HUMERAL STEM CEMENTED SIZE 12/130MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 19 | 10886982241535 | 5624-10/20XL | 56241020XL | COCR HUMERAL STEM CEMENTED SIZE 10/205MM XLONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 20 | 10886982241528 | 5624-10/16L | 56241016L | COCR HUMERAL STEM CEMENTED SIZE 10/165MM LONG-STERILE | NA | SYNTHES (U.S.A.) LP |
| 21 | 10886982241511 | 5624-10/12 | 56241012 | COCR HUMERAL STEM CEMENTED SIZE 10/125MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 22 | 10886982241467 | 5540-8/12 | 5540812 | TI HUMERAL STEM HA COATED PRESS-FIT SIZE 8/120MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 23 | 10886982241450 | 5540-6/11 | 5540611 | TI HUMERAL STEM HA COATED PRESS-FIT SIZE 6/115MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 24 | 10886982241443 | 5540-14/13 | 55401413 | TI HUMERAL STEM HA COATED PRESS-FIT SIZE 14/135MM-STER | NA | SYNTHES (U.S.A.) LP |
| 25 | 10886982241436 | 5540-12/13 | 55401213 | TI HUMERAL STEM HA COATED PRESS-FIT SIZE 12/130MM-STER | NA | SYNTHES (U.S.A.) LP |
| 26 | 10886982241429 | 5540-10/12 | 55401012 | TI HUMERAL STEM HA COATED PRESS-FIT SIZE 10/125MM-STER | NA | SYNTHES (U.S.A.) LP |
| 27 | 10886982241405 | 5537-8/12 | 5537812 | TI HUMERAL STEM PRESS-FIT SIZE 8/120MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 28 | 10886982241399 | 5537-6/11 | 5537611 | TI HUMERAL STEM PRESS-FIT SIZE 6/115MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 29 | 10886982241382 | 5537-14/13 | 55371413 | TI HUMERAL STEM PRESS-FIT SIZE 14/135MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 30 | 10886982241375 | 5537-12/13 | 55371213 | TI HUMERAL STEM PRESS-FIT SIZE 12/130MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 31 | 10886982241368 | 5537-10/12 | 55371012 | TI HUMERAL STEM PRESS-FIT SIZE 10/125MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 32 | 10886982241351 | 5413-20/6REV | 5413206REV | TI ECCENTER REVISION STANDARD STERILE | NA | SYNTHES (U.S.A.) LP |
| 33 | 10886982241344 | 5413-20/5-20 | 541320520 | TI ECCENTER REVISION +20 STERILE | NA | SYNTHES (U.S.A.) LP |
| 34 | 10886982241337 | 5413-20/5-15 | 541320515 | TI ECCENTER REVISION +15-STERILE | NA | SYNTHES (U.S.A.) LP |
| 35 | 10886982241320 | 5413-20/5-10 | 541320510 | TI ECCENTER REVISION +10 STERILE | NA | SYNTHES (U.S.A.) LP |
| 36 | 10886982241313 | 5413-20/5 | 5413205 | TI ECCENTER-STERILE | NA | SYNTHES (U.S.A.) LP |
| 37 | 10886982241306 | 5331-58/22 | 53315822 | COCR HEAD 58MM/21.75MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 38 | 10886982241290 | 5331-56/21 | 53315621 | COCR HEAD 56MM/21.00MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 39 | 10886982241283 | 5331-54/20 | 53315420 | COCR HEAD 54MM/20.25MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 40 | 10886982241276 | 5331-52/19 | 53315219 | COCR HEAD 52MM/19.50MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 41 | 10886982241269 | 5331-50/18 | 53315018 | COCR HEAD 50MM/18.75MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 42 | 10886982241252 | 5331-48/18 | 53314818 | COCR HEAD 48MM/18.00MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 43 | 10886982241245 | 5331-46/17 | 53314617 | COCR HEAD 46MM/17.25MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 44 | 10886982241238 | 5331-44/16 | 53314416 | COCR HEAD 44MM/16.50MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 45 | 10886982241221 | 5331-42/15 | 53314215 | COCR HEAD 42MM/15.75MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 46 | 10886982241214 | 5331-40/15 | 53314015 | COCR HEAD 40MM/15.00MM STERILE | NA | SYNTHES (U.S.A.) LP |
| 47 | 10886982239754 | 5213-58 | 521358 | GLENOID 58MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 48 | 10886982239747 | 5213-56 | 521356 | GLENOID 56MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 49 | 10886982239730 | 5213-54 | 521354 | GLENOID 54MM-STERILE | NA | SYNTHES (U.S.A.) LP |
| 50 | 10886982239723 | 5213-52 | 521352 | GLENOID 52MM-STERILE | NA | SYNTHES (U.S.A.) LP |