| 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 | 03700757200803 | KIT0708 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his | spineEOS rod Template | ONEFIT MEDICAL |
| 2 | 03700757200797 | KIT0707 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
| 3 | 03700757200780 | KIT0706 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
| 4 | 03700757200773 | KIT0705 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
| 5 | 03700757200766 | KIT0704 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
| 6 | 03700757200759 | KIT0703 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
| 7 | 03700757200650 | KIT0702 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
| 8 | 03700757200643 | KIT0701 | / | spineEOS rod template is intended to be designed from patient’s imaging data (EO spineEOS rod template is intended to be designed from patient’s imaging data (EOS images) in order to obtain a patient specific template, which allows to reproduce the shape of the planned spinal rods during surgery. Preoperative planning is performed and validated by surgeon with spineEOS software (provide a preoperative planning solution for spine surgeries). The template is designed from the output data of the software.This device is intended for guiding the surgeon during the bending of rods for spinal arthrodesis. However, in this context, the surgeon is the only one to determine whether patients can benefit from this technology according to his habits and his surgical experience. | spineEOS rod Template | ONEFIT MEDICAL |
| 9 | 03700386990014 | MWA255 | MWA255 | HUMERAL HEAD TRIAL | Aequalis Fracture | TORNIER |
| 10 | 03700386990007 | MWA254 | MWA254 | HUMERAL HEAD TRIAL | Aequalis Fracture | TORNIER |
| 11 | 03700386989834 | MWF339 | MWF339 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 12 | 03700386989827 | MWF337S | MWF337S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 13 | 03700386989810 | MWF337 | MWF337 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 14 | 03700386989759 | MWF255S | MWF255S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 15 | 03700386989742 | MWF255 | MWF255 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 16 | 03700386989735 | MWF254S | MWF254S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 17 | 03700386989728 | MWF254 | MWF254 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 18 | 03700386989711 | MWF237 | MWF237 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 19 | 03700386975547 | MWF355S | MWF355S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 20 | 03700386975530 | MWF355 | MWF355 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 21 | 03700386975523 | MWF354S | MWF354S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 22 | 03700386975516 | MWF354 | MWF354 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 23 | 03700386975509 | MWF353S | MWF353S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 24 | 03700386975493 | MWF353 | MWF353 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 25 | 03700386975486 | MWF352S | MWF352S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 26 | 03700386975479 | MWF352 | MWF352 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 27 | 03700386975462 | MWF351S | MWF351S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 28 | 03700386975455 | MWF351 | MWF351 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 29 | 03700386975448 | MWF350S | MWF350S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 30 | 03700386975431 | MWF350 | MWF350 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 31 | 03700386975424 | MWF348S | MWF348S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 32 | 03700386975417 | MWF348 | MWF348 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 33 | 03700386975400 | MWF346S | MWF346S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 34 | 03700386975394 | MWF346 | MWF346 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 35 | 03700386975387 | MWF343S | MWF343S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 36 | 03700386975370 | MWF343 | MWF343 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 37 | 03700386975363 | MWF341S | MWF341S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 38 | 03700386975356 | MWF341 | MWF341 | AEQUALIS™ HUMERAL HEAD XRo TRIAL | Tornier Flex | TORNIER |
| 39 | 03700386975349 | MWF339S | MWF339S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 40 | 03700386975332 | MWF253S | MWF253S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 41 | 03700386975318 | MWF252S | MWF252S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 42 | 03700386975295 | MWF251S | MWF251S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 43 | 03700386975271 | MWF250S | MWF250S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 44 | 03700386975257 | MWF248S | MWF248S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 45 | 03700386975233 | MWF246S | MWF246S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 46 | 03700386975219 | MWF243S | MWF243S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 47 | 03700386975196 | MWF241S | MWF241S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 48 | 03700386975172 | MWF239S | MWF239S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 49 | 03700386975158 | MWF237S | MWF237S | AEQUALIS™ HUMERAL HEAD TRIAL | Tornier Flex | TORNIER |
| 50 | 03700386974793 | MWF047 | MWF047 | Punch Template | Tornier Flex | TORNIER |