Other products from "DEPUY (IRELAND)"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 10603295261148 L93502 L93502 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
2 10603295261131 L93501 L93501 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
3 10603295547532 6505-36-008 650536008 INHANCE SHOULDER SYSTEM GLENOSPHERE TRIAL Ø36 +8mm HWT TEMPLATE 1 INHANCE
4 10603295539414 6205-10-104 620510104 INHANCE SHOULDER SYSTEM CONVEX IMPACTOR TIP HWA IMPACTOR 1 INHANCE
5 10603295525257 122128055 122128055 BI-MENTUM ALTRX LINER 55/28 LZO,MEH Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate 2 BI-MENTUM ALTRX
6 10603295515708 4831-36-015 483136015 TRIAL HEAD 36mm +1.5 HWT TEMPLATE 1 NA
7 10603295530725 2317-70-423 231770423 DELTA XTEND Peripheral locking screwdriver end cap with spring HXX SCREWDRIVER 1 DELTA XTEND
8 10603295524120 4800-00-210 480000210 EMPHASYS ACETABULAR ALUMINUM CADDY ANCILLARY FSM TRAY, SURGICAL, INSTRUMENT 1 EMPHASYS
9 10603295261629 L95092 L95092 KAR LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 KAR
10 10603295324508 L46818 L46818 Gyros Base Box 2 FSM TRAY, SURGICAL, INSTRUMENT 1 GYROS
11 10603295493549 2544-11-003 254411003 ATTUNE KNEE SYSTEM ATTUNE SYSTEM IMPACTOR HWA IMPACTOR 1 ATTUNE
12 10603295423324 2544-01-017 254401017 ATTUNE IMPACTION HANDLE HWA IMPACTOR 1 ATTUNE
13 10603295324539 L46844 L46844 GYROS LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 GYROS
14 10603295440574 2506-30-102 250630102 ATTUNE KNEE SYSTEM REVISION OFFSET DRILL HTW BIT, DRILL 1 ATTUNE
15 10603295434351 9505-05-171 950505171 Reach KNEE CASE 3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
16 10603295261346 L93554 L93554 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
17 10603295261704 L95122 L95122 PANIER 2 KAR FSM TRAY, SURGICAL, INSTRUMENT 1 NA
18 10603295423560 2545-01-706 254501706 ATTUNE PS TRIALS SIZE 6-8 FSM TRAY, SURGICAL, INSTRUMENT 1 ATTUNE
19 10603295261674 L95119 L95119 PLATEAU SYNOPTIQUE 1 KAR FSM TRAY, SURGICAL, INSTRUMENT 1 NA
20 10603295261667 L95099 L95099 KAR LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 KAR
21 10603295381105 1140-10-044 114010044 GLOBAL ICON Stemless Shoulder System Anchor Plate Size 44 HA PKC Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no Prosthesis, total anatomic shoulder, uncemented metaphyseal humeral stem with no diaphyseal incursion, semi-constrained 2 GLOBAL ICON
22 10603295285953 2407-42-209 240742209 DELTA CTA REV TRIAL CUP EPI36 D42 +9mm HWT TEMPLATE 1 DELTA CTA
23 10603295260295 L85878 L85878 TRAY 1 - INSERT 1 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
24 10603295243182 9625-75-000 962575000 ELITE FEMORAL HEAD +0 9/10 TAPER Diameter 32mm JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented 2 ELITE
25 10603295089612 2128-61-050 212861050 GLOBAL ADVANTAGE GLENOID CASE & INSERTS FSM TRAY, SURGICAL, INSTRUMENT 1 GLOBAL ADVANTAGE
26 10603295085508 2100-22-000 210022000 GLOBAL UNITE X-RAY TEMPLATES HWT TEMPLATE 1 GLOBAL UNITE
27 10603295077060 1976-17-190 197617190 RECLAIM REVISION HIP SYSTEM DISTAL TAPERED STEM 17mm X 190mm STRAIGHT LZO,KWA Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, semi-constrained (metal uncemented acetabular component) 2 RECLAIM
28 10603295043553 1513-12-110 151312110 ATTUNE KNEE SYSTEM REVISION PRESSFIT STEM 12X110MM MBH,JWH,NJL PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing 2 ATTUNE
29 10603295261087 L93384 L93384 TRAY No.1 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
30 10603295261070 L93383 L93383 TRAY COVER No.3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
31 10603295261063 L93382 L93382 TRAY COVER No.2 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
32 10603295261056 L93381 L93381 TRAY COVER No. 1 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
33 10603295261124 L93388 L93388 BOTTOM TRAY No. 3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
34 10603295261117 L93387 L93387 TOP TRAY , 3 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
35 10603295261100 L93386 L93386 BOTTOM TRAY No.2 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
36 10603295261094 L93385 L93385 TOP TRAY No.2 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
37 10603295261179 L93512 L93512 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
38 10603295261162 L93505 L93505 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
39 10603295261155 L93503 L93503 REEF LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 REEF
40 10603295548683 3010-01-090 301001090 ACTIS HIP SYSTEM BROACH SIZE 9 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
41 10603295548676 3010-01-080 301001080 ACTIS HIP SYSTEM BROACH SIZE 8 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
42 10603295548669 3010-01-070 301001070 ACTIS HIP SYSTEM BROACH SIZE 7 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
43 10603295548652 3010-01-060 301001060 ACTIS HIP SYSTEM BROACH SIZE 6 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
44 10603295548645 3010-01-050 301001050 ACTIS HIP SYSTEM BROACH SIZE 5 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
45 10603295548638 3010-01-040 301001040 ACTIS HIP SYSTEM BROACH SIZE 4 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
46 10603295548621 3010-01-030 301001030 ACTIS HIP SYSTEM BROACH SIZE 3 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
47 10603295548614 3010-01-020 301001020 ACTIS HIP SYSTEM BROACH SIZE 2 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
48 10603295548607 3010-01-120 301001120 ACTIS HIP SYSTEM BROACH SIZE 12 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
49 10603295548591 3010-01-110 301001110 ACTIS HIP SYSTEM BROACH SIZE 11 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
50 10603295548584 3010-01-100 301001100 ACTIS HIP SYSTEM BROACH SIZE 10 QBO Instruments designed for press-fit osteochondral implants 2 ACTIS
Other products with the same Product Codes "PHX, 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 08033390216418 9013.67.146 9013.67.146 PRIMA - Impactor Adaptor #6 PRIMA LIMACORPORATE SPA
8 08033390216418 9013.67.146 9013.67.146 PRIMA - Impactor Adaptor #6 PRIMA LIMACORPORATE SPA
9 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
10 08033390230599 9CCS.10.001 9CCS.10.001 ProMade shoulder 140° Reverse Resection Jig SMR Shoulder LIMACORPORATE SPA
11 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
12 08033390226172 9CCS.13.003 9CCS.13.003 Compactor S SMR Shoulder LIMACORPORATE SPA
13 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
14 08033390226165 9CCS.13.002 9CCS.13.002 Glenoid Drill Peg S SMR Shoulder LIMACORPORATE SPA
15 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 PRIMA LIMACORPORATE SPA
16 08033390216821 9013.67.067 9013.67.067 PRIMA - Metaphyseal Size ring #7 PRIMA LIMACORPORATE SPA
17 08033390216814 9013.67.066 9013.67.066 PRIMA - Metaphyseal Size ring #6 PRIMA LIMACORPORATE SPA
18 08033390216814 9013.67.066 9013.67.066 PRIMA - Metaphyseal Size ring #6 PRIMA LIMACORPORATE SPA
19 08033390216807 9013.67.064 9013.67.064 PRIMA - Metaphyseal Size ring #4 PRIMA LIMACORPORATE SPA
20 08033390216807 9013.67.064 9013.67.064 PRIMA - Metaphyseal Size ring #4 PRIMA LIMACORPORATE SPA
21 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
22 08033390216791 9013.67.065 9013.67.065 PRIMA - Metaphyseal Size ring #5 PRIMA LIMACORPORATE SPA
23 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
24 08033390216784 9013.67.063 9013.67.063 PRIMA - Metaphyseal Size ring #3 PRIMA LIMACORPORATE SPA
25 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
26 08033390216777 9013.67.062 9013.67.062 PRIMA - Metaphyseal Size ring #2 PRIMA LIMACORPORATE SPA
27 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
28 08033390216760 9013.67.061 9013.67.061 PRIMA - Metaphyseal Size ring #1 PRIMA LIMACORPORATE SPA
29 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
30 08033390216609 9013.67.140 9013.67.140 PRIMA - Impactor PRIMA LIMACORPORATE SPA
31 08033390216470 9013.67.141 9013.67.141 PRIMA - Impactor Adaptor #1 PRIMA LIMACORPORATE SPA
32 08033390216470 9013.67.141 9013.67.141 PRIMA - Impactor Adaptor #1 PRIMA LIMACORPORATE SPA
33 08033390216463 9013.67.055 9013.67.055 PRIMA - Metaphyseal Centering Guide - LEFT PRIMA LIMACORPORATE SPA
34 08033390216463 9013.67.055 9013.67.055 PRIMA - Metaphyseal Centering Guide - LEFT PRIMA LIMACORPORATE SPA
35 08033390216456 9013.67.050 9013.67.050 PRIMA - Metaphyseal Centering Guide - RIGHT PRIMA LIMACORPORATE SPA
36 08033390216456 9013.67.050 9013.67.050 PRIMA - Metaphyseal Centering Guide - RIGHT PRIMA LIMACORPORATE SPA
37 08033390216432 9013.67.147 9013.67.147 PRIMA - Impactor Adaptor #7 PRIMA LIMACORPORATE SPA
38 08033390216432 9013.67.147 9013.67.147 PRIMA - Impactor Adaptor #7 PRIMA LIMACORPORATE SPA
39 08033390216401 9013.67.145 9013.67.145 PRIMA - Impactor Adaptor #5 PRIMA LIMACORPORATE SPA
40 08033390216401 9013.67.145 9013.67.145 PRIMA - Impactor Adaptor #5 PRIMA LIMACORPORATE SPA
41 08033390216395 9013.67.144 9013.67.144 PRIMA - Impactor Adaptor #4 PRIMA LIMACORPORATE SPA
42 08033390216395 9013.67.144 9013.67.144 PRIMA - Impactor Adaptor #4 PRIMA LIMACORPORATE SPA
43 08033390216333 9013.67.143 9013.67.143 PRIMA - Impactor Adaptor #3 PRIMA LIMACORPORATE SPA
44 08033390216333 9013.67.143 9013.67.143 PRIMA - Impactor Adaptor #3 PRIMA LIMACORPORATE SPA
45 08033390216326 9013.67.142 9013.67.142 PRIMA - Impactor Adaptor #2 PRIMA LIMACORPORATE SPA
46 08033390216326 9013.67.142 9013.67.142 PRIMA - Impactor Adaptor #2 PRIMA LIMACORPORATE SPA
47 08033390215763 9013.74.151 9013.74.151 SMR - Ecc. Glenosphere Orienter 42mm SMR Shoulder LIMACORPORATE SPA
48 08033390215763 9013.74.151 9013.74.151 SMR - Ecc. Glenosphere Orienter 42mm SMR Shoulder LIMACORPORATE SPA
49 08033390215756 9013.74.150 9013.74.150 SMR - Glenosphere Orienter 42mm SMR Shoulder LIMACORPORATE SPA
50 08033390215756 9013.74.150 9013.74.150 SMR - Glenosphere Orienter 42mm SMR Shoulder LIMACORPORATE SPA