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 | 00845694094658 | 231-2828T | 231-2828T | Large, Prebent Recon TEMPLATE, ICON | OsteoMed | OSTEOMED LLC |
2 | 00845694094641 | 231-2826T | 231-2826T | Medium, Prebent Recon TEMPLATE, ICON | OsteoMed | OSTEOMED LLC |
3 | 00845694094634 | 231-2824T | 231-2824T | Small, Prebent Recon TEMPLATE, ICON | OsteoMed | OSTEOMED LLC |
4 | 00844868040835 | RT-EZTETIC | RADIOGRAPHIC TRANSPARENCY FOR EZTETIC™ DENTAL IMPLANTS | NA | BIOMET 3I, LLC | |
5 | 00844868040828 | RT-BTAP | RADIOGRAPHIC TRANSPARENCY FOR BIOMET 3I TAPERED IMPLANTS | NA | BIOMET 3I, LLC | |
6 | 00844868040811 | RT-BPW | RADIOGRAPHIC TRANSPARENCY FOR BIOMET 3I PARALLEL WALLED IMPLANTS | NA | BIOMET 3I, LLC | |
7 | 00844868040880 | RT-TSV | RADIOGRAPHIC TRANSPARENCY FOR TAPERED SCREW-VENT® IMPLANTS | NA | BIOMET 3I, LLC | |
8 | 00844868040873 | RT-SWISSPLT | RADIOGRAPHIC TRANSPARENCY FOR TAPERED SWISSPLUS® IMPLANTS | NA | BIOMET 3I, LLC | |
9 | 00844868040842 | RT-SPLINE | RADIOGRAPHIC TRANSPARENCY FOR SPLINE® IMPLANTS | NA | BIOMET 3I, LLC | |
10 | 00844868038245 | RT-SHIMP | RADIOGRAPHIC TRANSPARENCY FOR T3® SHORT IMPLANTS | NA | BIOMET 3I, LLC | |
11 | 00844856069831 | 87040 | BRIDGE GAUGE | Arsenal | ALPHATEC SPINE, INC. | |
12 | 00844856069626 | 87015-500 | 500mm ROD TEMPLATE | Arsenal | ALPHATEC SPINE, INC. | |
13 | 00844856069619 | 87015-250 | 250mm ROD TEMPLATE | Arsenal | ALPHATEC SPINE, INC. | |
14 | 00844856069602 | 87015-130 | 130mm ROD TEMPLATE | Arsenal | ALPHATEC SPINE, INC. | |
15 | 00844856044180 | 73744 | GUIDEWIRE MEASUREMENT RULER | Illico | ALPHATEC SPINE, INC. | |
16 | 00844856044104 | 73727 | ROD TEMPLATE | Illico | ALPHATEC SPINE, INC. | |
17 | 00844856026780 | 62930-45 | ROD TEMPLATE 45cm LENGTH 5mm DIA | Zodiac | ALPHATEC SPINE, INC. | |
18 | 00844856026773 | 62930-15 | ROD TEMPLATE 15cm LENGTH 5mm DIA | Zodiac | ALPHATEC SPINE, INC. | |
19 | 00844856007697 | 63924-15 | 3.0mm ROD TEMPLATE, 15cm | Solanas | ALPHATEC SPINE, INC. | |
20 | 00844856006072 | 62936 | SCREW MEASUREMENT BLOCK | Zodiac | ALPHATEC SPINE, INC. | |
21 | 00843575112552 | 8829P00004 | 8829P00004 | Femoral AR Sizer | AR Specialty Femoral | B-ONE ORTHO, CORP. |
22 | 00843575112361 | 8829P00046 | 8829P00046 | Femoral Prep Guide, Long | AR Specialty Femoral | B-ONE ORTHO, CORP. |
23 | 00843575112354 | 8829P00045 | 8829P00045 | Femoral Prep Guide, Short | AR Specialty Femoral | B-ONE ORTHO, CORP. |
24 | 00843575112347 | 8829P00001 | 8829P00001 | Femoral Prep Guide, Standard | AR Specialty Femoral | B-ONE ORTHO, CORP. |
25 | 00843575111043 | 8819000016 | 8819000016 | FEMORAL RESECTION GUIDE | Kosmo Femoral Hip System | B-ONE ORTHO, CORP. |
26 | 00843575108708 | 8829102400 | 8829102400 | Adjustable Distal Resection Tower | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
27 | 00843575108685 | 8829101120 | 8829101120 | Distal Femoral Alignment Guide | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
28 | 00843575106438 | 8829202000 | 8829202000 | EM Tibial Alignment Guide, Non-Spiked Uprod, Standard | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
29 | 00843575106421 | 8829201000 | 8829201000 | EM Tibial Alignment Guide, Spiked Uprod, Standard | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
30 | 00843575104748 | 8829102200 | 8829102200 | Adjustable Distal Resection Guide Tower | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
31 | 00843575104441 | 8829402000 | 8829402000 | Patella Sizer | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
32 | 00843575104328 | 8829206000 | 8829206000 | IM Tibial Alignment Guide | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
33 | 00843575104298 | 8829202100 | 8829202100 | EM Tibial Alignment Guide, Non-Spiked Uprod, Long | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
34 | 00843575104281 | 8829201100 | 8829201100 | EM Tibial Alignment Guide, Spiked Uprod, Long | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
35 | 00843575104274 | 8829200000 | 8829200000 | EM Tibial Alignment Guide, Base | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
36 | 00843575104243 | 8829102000 | 8829102000 | Fixed Distal Resection Guide Tower | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
37 | 00843575104236 | 8829101200 | 8829101200 | Epicondylar Guide | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
38 | 00843575104229 | 8829101100 | 8829101100 | Distal Femoral Alignment Guide | MOBIO™ Total Knee System | B-ONE ORTHO, CORP. |
39 | 00843575104106 | 881906436L | 881906436L | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE L X 36MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
40 | 00843575104090 | 881906436K | 881906436K | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE K X 36MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
41 | 00843575104083 | 881906436J | 881906436J | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE J X 36MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
42 | 00843575104076 | 881906436I | 881906436I | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE I X 36MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
43 | 00843575104069 | 881906432I | 881906432I | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE I X 32MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
44 | 00843575104052 | 881906436H | 881906436H | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE H X 36MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
45 | 00843575104045 | 881906432H | 881906432H | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE H X 32MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
46 | 00843575104038 | 881906436G | 881906436G | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE G X 36MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
47 | 00843575104021 | 881906432G | 881906432G | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE G X 32MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
48 | 00843575104014 | 881906428G | 881906428G | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE G X 28MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
49 | 00843575104007 | 881906432F | 881906432F | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE F X 32MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |
50 | 00843575103994 | 881906428F | 881906428F | ACETABULAR LINER TRIAL, HOODED, 10 degree, SIZE F X 28MM I.D. | b-ONE™ Primary Acetabular System | B-ONE ORTHO, CORP. |