Other products from "ZIMMER, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024233638 42-5112-004-10 42-5112-004-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
2 00889024233621 42-5112-003-20 42-5112-003-20 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
3 00889024233614 42-5112-003-18 42-5112-003-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
4 00889024233607 42-5112-003-16 42-5112-003-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
5 00889024233591 42-5112-003-14 42-5112-003-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
6 00889024233584 42-5112-003-13 42-5112-003-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
7 00889024233577 42-5112-003-12 42-5112-003-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
8 00889024233560 42-5112-003-11 42-5112-003-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
9 00889024233553 42-5112-003-10 42-5112-003-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
10 00889024233546 42-5112-002-20 42-5112-002-20 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
11 00889024233539 42-5112-002-18 42-5112-002-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
12 00889024233522 42-5112-002-16 42-5112-002-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
13 00889024233515 42-5112-002-14 42-5112-002-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
14 00889024233508 42-5112-002-13 42-5112-002-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
15 00889024233492 42-5112-002-12 42-5112-002-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
16 00889024233485 42-5112-002-11 42-5112-002-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
17 00889024233478 42-5112-002-10 42-5112-002-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
18 00889024233461 42-5112-001-20 42-5112-001-20 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
19 00889024233454 42-5112-001-18 42-5112-001-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
20 00889024233447 42-5112-001-16 42-5112-001-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
21 00889024233430 42-5112-001-14 42-5112-001-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
22 00889024233423 42-5112-001-13 42-5112-001-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
23 00889024233416 42-5112-001-12 42-5112-001-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
24 00889024233409 42-5112-001-11 42-5112-001-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
25 00889024233393 42-5112-001-10 42-5112-001-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
26 00889024233386 42-5110-007-18 42-5110-007-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
27 00889024233379 42-5110-007-16 42-5110-007-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
28 00889024233362 42-5110-007-14 42-5110-007-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
29 00889024233355 42-5110-007-13 42-5110-007-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
30 00889024233348 42-5110-007-12 42-5110-007-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
31 00889024233331 42-5110-007-11 42-5110-007-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
32 00889024233324 42-5110-007-10 42-5110-007-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
33 00889024233317 42-5110-006-18 42-5110-006-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
34 00889024233300 42-5110-006-16 42-5110-006-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
35 00889024233294 42-5110-006-14 42-5110-006-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
36 00889024233287 42-5110-006-13 42-5110-006-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
37 00889024233270 42-5110-006-12 42-5110-006-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
38 00889024233263 42-5110-006-11 42-5110-006-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
39 00889024233256 42-5110-006-10 42-5110-006-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
40 00889024233249 42-5110-005-18 42-5110-005-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
41 00889024233232 42-5110-005-16 42-5110-005-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
42 00889024233225 42-5110-005-14 42-5110-005-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
43 00889024233218 42-5110-005-13 42-5110-005-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
44 00889024233201 42-5110-005-12 42-5110-005-12 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
45 00889024233195 42-5110-005-11 42-5110-005-11 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
46 00889024233188 42-5110-005-10 42-5110-005-10 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
47 00889024233171 42-5110-004-18 42-5110-004-18 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
48 00889024233164 42-5110-004-16 42-5110-004-16 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
49 00889024233157 42-5110-004-14 42-5110-004-14 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
50 00889024233140 42-5110-004-13 42-5110-004-13 JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 PERSONA™
Other products with the same Product Codes "KWT, KWS"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08058964726087 900001 144818 "Disposable cement spacer molds with metal reinforcement stem are indicated for "Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge." SpaceFlex Shoulder G21 SRL
2 08058964726070 900001 124818 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
3 08058964726063 900001 124215 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
4 08058964726056 900001 104818 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
5 08058964726049 900001 104215 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
6 08058964724977 900001 084215 Disposable cement spacer molds with metal reinforcement stem are indicated for u Disposable cement spacer molds with metal reinforcement stem are indicated for use to mold atemporary hemi- shoulder replacement for skeletally mature patients undergoing a two-stagerevision procedure due to a septic process.The temporary prosthesis is molded using low viscosity polymethylmethacrylate bonecement and inserted into the humeral medullary canal and glenoid cavity of the shoulderfollowing removal of the existing humeral and glenoideal cavity implants and debridement.SpaceFlex Shoulder should only be used with G3A low-viscosity bone cement.The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy(standard treatment approach to an infection).The hemi-shoulder prosthesis made from the SpaceFlex Shoulder disposable cement molds isnot intended for use more than 180 days, at which time it must be explanted and permanentdevices implanted or another appropriate treatment performed (e.g. resection arthroplasty,fusion, etc.).Due to the inherent mechanical limitations of the hemi-shoulder prosthesis material (lowviscosity polymethylmethacrylate), the temporary hemi-shoulder prosthesis is only indicatedfor patients who will consistently follow activity limitation throughout the implant period.The device can exclusively be used by competent healthcare personnel who has completescientific and anatomical knowledge. SpaceFlex Shoulder G21 SRL
7 08033390244640 9CC0.13.03B 9CC0.13.03B Glenoid Drilling Guide Dia. 2,7 mm ProMade LIMACORPORATE SPA
8 08033390237420 9CC0.13.03E 9CC0.13.03E M8 Long Handle ProMade LIMACORPORATE SPA
9 08033390237406 9CC0.13.03C 9CC0.13.03C M8 Handle with Flange ProMade LIMACORPORATE SPA
10 08033390237338 9CC0.13.038 9CC0.13.038 Glenoid Drilling Guide - Dia. 3.2 mm Drill ProMade LIMACORPORATE SPA
11 08033390216418 9013.67.146 9013.67.146 PRIMA - Impactor Adaptor #6 PRIMA LIMACORPORATE SPA
12 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
13 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
14 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
15 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
16 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
17 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
18 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 PRIMA LIMACORPORATE SPA
19 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 PRIMA LIMACORPORATE SPA
20 08033390216814 9013.67.066 9013.67.066 PRIMA - Metaphyseal Size ring #6 PRIMA LIMACORPORATE SPA
21 08033390216814 9013.67.066 9013.67.066 PRIMA - Metaphyseal Size ring #6 PRIMA LIMACORPORATE SPA
22 08033390216807 9013.67.064 9013.67.064 PRIMA - Metaphyseal Size ring #4 PRIMA LIMACORPORATE SPA
23 08033390216807 9013.67.064 9013.67.064 PRIMA - Metaphyseal Size ring #4 PRIMA LIMACORPORATE SPA
24 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
25 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
26 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
27 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
28 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
29 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
30 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
31 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
32 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
33 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
34 08033390216470 9013.67.141 9013.67.141 PRIMA - Impactor Adaptor #1 PRIMA LIMACORPORATE SPA
35 08033390216470 9013.67.141 9013.67.141 PRIMA - Impactor Adaptor #1 PRIMA LIMACORPORATE SPA
36 08033390216463 9013.67.055 9013.67.055 PRIMA - Metaphyseal Centering Guide - LEFT PRIMA LIMACORPORATE SPA
37 08033390216463 9013.67.055 9013.67.055 PRIMA - Metaphyseal Centering Guide - LEFT PRIMA LIMACORPORATE SPA
38 08033390216456 9013.67.050 9013.67.050 PRIMA - Metaphyseal Centering Guide - RIGHT PRIMA LIMACORPORATE SPA
39 08033390216456 9013.67.050 9013.67.050 PRIMA - Metaphyseal Centering Guide - RIGHT PRIMA LIMACORPORATE SPA
40 08033390216432 9013.67.147 9013.67.147 PRIMA - Impactor Adaptor #7 PRIMA LIMACORPORATE SPA
41 08033390216432 9013.67.147 9013.67.147 PRIMA - Impactor Adaptor #7 PRIMA LIMACORPORATE SPA
42 08033390216418 9013.67.146 9013.67.146 PRIMA - Impactor Adaptor #6 PRIMA LIMACORPORATE SPA
43 08033390216401 9013.67.145 9013.67.145 PRIMA - Impactor Adaptor #5 PRIMA LIMACORPORATE SPA
44 08033390216401 9013.67.145 9013.67.145 PRIMA - Impactor Adaptor #5 PRIMA LIMACORPORATE SPA
45 08033390216395 9013.67.144 9013.67.144 PRIMA - Impactor Adaptor #4 PRIMA LIMACORPORATE SPA
46 08033390216395 9013.67.144 9013.67.144 PRIMA - Impactor Adaptor #4 PRIMA LIMACORPORATE SPA
47 08033390216333 9013.67.143 9013.67.143 PRIMA - Impactor Adaptor #3 PRIMA LIMACORPORATE SPA
48 08033390216333 9013.67.143 9013.67.143 PRIMA - Impactor Adaptor #3 PRIMA LIMACORPORATE SPA
49 08033390216326 9013.67.142 9013.67.142 PRIMA - Impactor Adaptor #2 PRIMA LIMACORPORATE SPA
50 08033390216326 9013.67.142 9013.67.142 PRIMA - Impactor Adaptor #2 PRIMA LIMACORPORATE SPA