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 |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 04260102136977 | knee L | 5034796 | The COPAL® exchange G Hip and Knee Spacers devices provide patients, undergoing The COPAL® exchange G Hip and Knee Spacers devices provide patients, undergoing a two-stage revision procedure for an infected total joint, a temporary implant to l) allow for partial weight bearing and 2) provide an approximate natural range of motion. The devices also maintain a patient's soft tissue and joint space, preventing further complications such as muscular contraction. The gentamicin protects the device from bacterial colonization.The COPAL® exchange G Hip and Knee Spacers are placed into the joint to maintain normal joint space and alignment. They provide patient comfort and limited mobility while the infection is being treated. The COPAL® exchange G Hip and Knee Spacers are made with bone cement that are loaded with gentamicin antibiotics.The COPAL® exchange G Hip and Knee Spacers are temporary joint prostheses designed to temporarily replace an infected implant during a total hip or knee arthroplasty and provide the patient with limited mobility and predictable, consistent local antibiotic release. | COPAL® exchange G | HERAEUS MEDICAL GMBH |
2 | 04260102136946 | knee M | 5034797 | The COPAL® exchange G Hip and Knee Spacers devices provide patients, undergoing The COPAL® exchange G Hip and Knee Spacers devices provide patients, undergoing a two-stage revision procedure for an infected total joint, a temporary implant to l) allow for partial weight bearing and 2) provide an approximate natural range of motion. The devices also maintain a patient's soft tissue and joint space, preventing further complications such as muscular contraction. The gentamicin protects the device from bacterial colonization.The COPAL® exchange G Hip and Knee Spacers are placed into the joint to maintain normal joint space and alignment. They provide patient comfort and limited mobility while the infection is being treated. The COPAL® exchange G Hip and Knee Spacers are made with bone cement that are loaded with gentamicin antibiotics.The COPAL® exchange G Hip and Knee Spacers are temporary joint prostheses designed to temporarily replace an infected implant during a total hip or knee arthroplasty and provide the patient with limited mobility and predictable, consistent local antibiotic release. | COPAL® exchange G | HERAEUS MEDICAL GMBH |
3 | 04260102136915 | knee S | 5034798 | The COPAL® exchange G Hip and Knee Spacers devices provide patients, undergoing The COPAL® exchange G Hip and Knee Spacers devices provide patients, undergoing a two-stage revision procedure for an infected total joint, a temporary implant to l) allow for partial weight bearing and 2) provide an approximate natural range of motion. The devices also maintain a patient's soft tissue and joint space, preventing further complications such as muscular contraction. The gentamicin protects the device from bacterial colonization.The COPAL® exchange G Hip and Knee Spacers are placed into the joint to maintain normal joint space and alignment. They provide patient comfort and limited mobility while the infection is being treated. The COPAL® exchange G Hip and Knee Spacers are made with bone cement that are loaded with gentamicin antibiotics.The COPAL® exchange G Hip and Knee Spacers are temporary joint prostheses designed to temporarily replace an infected implant during a total hip or knee arthroplasty and provide the patient with limited mobility and predictable, consistent local antibiotic release. | COPAL® exchange G | HERAEUS MEDICAL GMBH |
4 | 04046964452062 | NX353 | NX353 | ALL POLY TIBIA VEGA PS T5 16MM | VEGA System® PS | AESCULAP AG |
5 | 04046964452055 | NX352 | NX352 | ALL POLY TIBIA VEGA PS T5 14MM | VEGA System® PS | AESCULAP AG |
6 | 04046964452048 | NX351 | NX351 | ALL POLY TIBIA VEGA PS T5 12MM | VEGA System® PS | AESCULAP AG |
7 | 04046964452031 | NX350 | NX350 | ALL POLY TIBIA VEGA PS T5 10MM | VEGA System® PS | AESCULAP AG |
8 | 04046964452024 | NX343 | NX343 | ALL POLY TIBIA VEGA PS T4 16MM | VEGA System® PS | AESCULAP AG |
9 | 04046964452017 | NX342 | NX342 | ALL POLY TIBIA VEGA PS T4 14MM | VEGA System® PS | AESCULAP AG |
10 | 04046964452000 | NX341 | NX341 | ALL POLY TIBIA VEGA PS T4 12MM | VEGA System® PS | AESCULAP AG |
11 | 04046964451911 | NX322 | NX322 | ALL POLY TIBIA VEGA PS T2 14MM | VEGA System® PS | AESCULAP AG |
12 | 04046964451904 | NX321 | NX321 | ALL POLY TIBIA VEGA PS T2 12MM | VEGA System® PS | AESCULAP AG |
13 | 04046964451898 | NX320 | NX320 | ALL POLY TIBIA VEGA PS T2 10MM | VEGA System® PS | AESCULAP AG |
14 | 04046964451881 | NX313 | NX313 | ALL POLY TIBIA VEGA PS T1 16MM | VEGA System® PS | AESCULAP AG |
15 | 04046964451874 | NX312 | NX312 | ALL POLY TIBIA VEGA PS T1 14MM | VEGA System® PS | AESCULAP AG |
16 | 04046964451867 | NX311 | NX311 | ALL POLY TIBIA VEGA PS T1 12MM | VEGA System® PS | AESCULAP AG |
17 | 04046964451850 | NX310 | NX310 | ALL POLY TIBIA VEGA PS T1 10MM | VEGA System® PS | AESCULAP AG |
18 | 04046964451843 | NX303 | NX303 | ALL POLY TIBIA VEGA PS T0 16MM | VEGA System® PS | AESCULAP AG |
19 | 04046964451836 | NX302 | NX302 | ALL POLY TIBIA VEGA PS T0 14MM | VEGA System® PS | AESCULAP AG |
20 | 04046964451829 | NX301 | NX301 | ALL POLY TIBIA VEGA PS T0 12MM | VEGA System® PS | AESCULAP AG |
21 | 04046964451812 | NX300 | NX300 | ALL POLY TIBIA VEGA PS T0 10MM | VEGA System® PS | AESCULAP AG |
22 | 04046964451751 | NN1253 | NN1253 | ALL POLY TIBIA COLUMBUS CR DD T5 16MM | Columbus® CR DD | AESCULAP AG |
23 | 04046964451744 | NN1252 | NN1252 | ALL POLY TIBIA COLUMBUS CR DD T5 14MM | Columbus® CR DD | AESCULAP AG |
24 | 04046964451737 | NN1251 | NN1251 | ALL POLY TIBIA COLUMBUS CR DD T5 12MM | Columbus® CR DD | AESCULAP AG |
25 | 04046964451720 | NN1250 | NN1250 | ALL POLY TIBIA COLUMBUS CR DD T5 10MM | Columbus® CR DD | AESCULAP AG |
26 | 04046964451713 | NN1243 | NN1243 | ALL POLY TIBIA COLUMBUS CR DD T4 16MM | Columbus® CR DD | AESCULAP AG |
27 | 04046964451706 | NN1242 | NN1242 | ALL POLY TIBIA COLUMBUS CR DD T4 14MM | Columbus® CR DD | AESCULAP AG |
28 | 04046964451690 | NN1241 | NN1241 | ALL POLY TIBIA COLUMBUS CR DD T4 12MM | Columbus® CR DD | AESCULAP AG |
29 | 04046964451683 | NN1240 | NN1240 | ALL POLY TIBIA COLUMBUS CR DD T4 10MM | Columbus® CR DD | AESCULAP AG |
30 | 04046964451676 | NN1233 | NN1233 | ALL POLY TIBIA COLUMBUS CR DD T3 16MM | Columbus® CR DD | AESCULAP AG |
31 | 04046964451669 | NN1232 | NN1232 | ALL POLY TIBIA COLUMBUS CR DD T3 14MM | Columbus® CR DD | AESCULAP AG |
32 | 04046964451652 | NN1231 | NN1231 | ALL POLY TIBIA COLUMBUS CR DD T3 12MM | Columbus® CR DD | AESCULAP AG |
33 | 04046964451645 | NN1230 | NN1230 | ALL POLY TIBIA COLUMBUS CR DD T3 10MM | Columbus® CR DD | AESCULAP AG |
34 | 04046964451638 | NN1223 | NN1223 | ALL POLY TIBIA COLUMBUS CR DD T2 16MM | Columbus® CR DD | AESCULAP AG |
35 | 04046964451621 | NN1222 | NN1222 | ALL POLY TIBIA COLUMBUS CR DD T2 14MM | Columbus® CR DD | AESCULAP AG |
36 | 04046964451614 | NN1221 | NN1221 | ALL POLY TIBIA COLUMBUS CR DD T2 12MM | Columbus® CR DD | AESCULAP AG |
37 | 04046964451607 | NN1220 | NN1220 | ALL POLY TIBIA COLUMBUS CR DD T2 10MM | Columbus® CR DD | AESCULAP AG |
38 | 04046964451591 | NX340 | NX340 | ALL POLY TIBIA VEGA PS T4 10MM | VEGA System® PS | AESCULAP AG |
39 | 04046964451584 | NX333 | NX333 | ALL POLY TIBIA VEGA PS T3 16MM | VEGA System® PS | AESCULAP AG |
40 | 04046964451577 | NX332 | NX332 | ALL POLY TIBIA VEGA PS T3 14MM | VEGA System® PS | AESCULAP AG |
41 | 04046964451560 | NX331 | NX331 | ALL POLY TIBIA VEGA PS T3 12MM | VEGA System® PS | AESCULAP AG |
42 | 04046964451553 | NX330 | NX330 | ALL POLY TIBIA VEGA PS T3 10MM | VEGA System® PS | AESCULAP AG |
43 | 04046964451546 | NX323 | NX323 | ALL POLY TIBIA VEGA PS T2 16MM | VEGA System® PS | AESCULAP AG |
44 | 04046964449994 | NN1213 | NN1213 | ALL POLY TIBIA COLUMBUS CR DD T1 16MM | Columbus® CR DD | AESCULAP AG |
45 | 04046964449987 | NN1212 | NN1212 | ALL POLY TIBIA COLUMBUS CR DD T1 14MM | Columbus® CR DD | AESCULAP AG |
46 | 04046964449970 | NN1211 | NN1211 | ALL POLY TIBIA COLUMBUS CR DD T1 12MM | Columbus® CR DD | AESCULAP AG |
47 | 04046964449963 | NN1210 | NN1210 | ALL POLY TIBIA COLUMBUS CR DD T1 10MM | Columbus® CR DD | AESCULAP AG |
48 | 04046964449956 | NN1203 | NN1203 | ALL POLY TIBIA COLUMBUS CR DD T0 16MM | Columbus® CR DD | AESCULAP AG |
49 | 04046964449949 | NN1202 | NN1202 | ALL POLY TIBIA COLUMBUS CR DD T0 14MM | Columbus® CR DD | AESCULAP AG |
50 | 04046964449932 | NN1201 | NN1201 | ALL POLY TIBIA COLUMBUS CR DD T0 12MM | Columbus® CR DD | AESCULAP AG |