No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00885556051375 | 71930717 | 71930717 | SYNERGY PC FEM SZ18 130MM | LPH | PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED | 2 | SYNERGY |
2 | 00885556799789 | 71075113B | 71075113B | SMART TSF FULL RING 130MM BLUE | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | SMART TSF |
3 | 00885556765357 | E0016663-6 | E0016663-6 | HANDLE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
4 | 00885556076538 | 913374 | 913374 | STAPLE 1.16X3.8X3.4 | JDR | STAPLE, FIXATION, BONE | 2 | NA |
5 | 00885556885208 | E0017815-2 | E0017815-2 | SHORTENED 180 2/3 RING | JDW | PIN, FIXATION, THREADED | 2 | Ex-Fix |
6 | 00885556883051 | E0017793-1 | E0017793-1 | MODIFIED META NAIL DROP | HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES | 2 | Meta Nail |
7 | 00885556867969 | E0017558-7 | E0017558-7 | FLEXIBLE I/M ROD | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Journey II |
8 | 00885556816721 | E0017448-3 | E0017448-3 | MODIFIED HEX DRIVER | HWR | DRIVER, PROSTHESIS | 1 | Polar |
9 | 00885556810484 | E0017443-1 | E0017443-1 | JII TIBIAL BLOCK - LEFT | FZX | Guide, surgical, instrument | 1 | JII |
10 | 00885556806326 | E0017367-11 | E0017367-11 | MODIFIED R3 INSERTER | JDI | Prosthesis, hip, semi-constrained, metal/polymer, cemented | 2 | R3 |
11 | 00885556805770 | E0017337-1 | E0017337-1 | JII FLEXION SPACER BLOCK | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | JII |
12 | 00885556804827 | E0017314-9 | E0017314-9 | AP BLOCK SZ 8 | FZX | Guide, surgical, instrument | 1 | Legion |
13 | 00885556802410 | E0017267-1 | E0017267-1 | TIBIAL STEM TRIAL - 10MM X 70MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Legion |
14 | 00885556801673 | E0017241-1 | E0017241-1 | MIS DA X-BAR | JDG | Prosthesis, hip, femoral component, cemented, metal | 2 | R3 |
15 | 00885556800812 | E0017230-1 | E0017230-1 | 2MM RECUT BLOCK | HWT | TEMPLATE | 1 | Journey II |
16 | 00885556795255 | E0017150-1 | E0017150-1 | 11MM DEEP FLUTED END CUTTING REAMER | HTO | REAMER | 1 | Trigen |
17 | 00885556793893 | E0017119-7 | E0017119-7 | MIS ACETABULAR REAMER 58MM | HTO | REAMER | 1 | R3 |
18 | 00885556791905 | E0017091-2 | E0017091-2 | TIBIAL CUTTING BLOCK - RT | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
19 | 00885556790229 | E0017054-1 | E0017054-1 | MODULAR FIN PUNCH HANDLE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | JII |
20 | 00885556783313 | E0016980-3 | E0016980-3 | UPPER TIBIAL GUIDE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Journey II |
21 | 00885556777954 | E0016892-1 | E0016892-1 | 9MM REAMER HEAD | HTO | REAMER | 1 | Trigen |
22 | 00885556775103 | E0016853-3 | E0016853-3 | EXTENDED T8 DRIVER SHAFT | HXX | SCREWDRIVER | 1 | PERI-LOC |
23 | 00885556773673 | ROB20000 | ROB20000 | CORI ROBOTICS USA | OLO | Orthopedic stereotaxic instrument | 2 | Real Intelligence |
24 | 00885556771013 | E0016765-1 | E0016765-1 | MODIFIED ANGEL WING | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
25 | 00885556770566 | E0016753-1 | E0016753-1 | FLUTED CURVED CANNULATED AWL | HWJ | AWL | 1 | Trigen |
26 | 00885556763742 | 71170734 | 71170734 | EVOS LARGE PROXIMAL HUMERUS PLATE TRAY | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | EVOS |
27 | 00885556763155 | E0016528-7 | E0016528-7 | SZ 51MM BRIDGEBACK REAMER | HTO | REAMER | 1 | R3 |
28 | 00885556762189 | 72581004 | 72581004 | EVOS 3.5MM/4.5MM UTILITY PLATE 4H 147MM | HRS | Plate, fixation, bone | 2 | EVOS |
29 | 00885556757192 | E0016586-2 | E0016586-2 | 8.5MM REAMER HEAD | HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT | 1 | Trigen |
30 | 00885556757116 | E0016583-1 | E0016583-1 | RAT TAIL RASP | JDG | Prosthesis, hip, femoral component, cemented, metal | 2 | Polar |
31 | 00885556755068 | ROB10000 | ROB10000 | CORI Starter Kit | OLO | Orthopedic stereotaxic instrument | 2 | CORI |
32 | 00885556753682 | E0016536-2 | E0016536-2 | ZUK SPACER BLOCK - 11MM | HWT | TEMPLATE | 1 | Uni |
33 | 00885556752081 | 72546585N | 72546585N | EVOS 6.5MM X 85MM CANNULATED SCREW | HWC | Screw, fixation, bone | 2 | EVOS |
34 | 00885556740422 | E0016327-2 | E0016327-2 | IM ROD SHORT | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | JII |
35 | 00885556737392 | E0016303-3 | E0016303-3 | OFFSET FIXATION ROD | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | JII |
36 | 00885556733837 | E0016253-2 | E0016253-2 | LARGE BLADE | GAD | RETRACTOR | 1 | Anthology |
37 | 00885556725337 | E0016116-2 | E0016116-2 | 2MM RECUT BLOCK | HWT | TEMPLATE | 1 | Legion |
38 | 00885556722701 | 21-8020 | 21-8020 | DEPTH GAGE | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | N/A |
39 | 00885556627020 | PFSI00040 | PFSI00040 | Stride Poly Insert Size D 9mm | HSX | PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | STRIDE |
40 | 00885556716274 | E0015966-1 | E0015966-1 | FEMORAL STYLUS | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
41 | 00885556715536 | E0015722-1 | E0015722-1 | FEMORAL TRIAL PADDLE | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
42 | 00885556626979 | PFSI00033 | PFSI00033 | Stride Poly Insert Size C 8mm | HSX | PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | STRIDE |
43 | 00885556713662 | 72411812 | 72411812 | EVOS 1.8MM X 12MM LOCKING PEG T7 | HRS | Plate, fixation, bone | 2 | EVOS |
44 | 00885556710357 | E0015809-1 | E0015809-1 | SIDE FEMORAL HEAD IMPACTOR | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | R3 |
45 | 00885556710418 | E0015860-1 | E0015860-1 | IM ALIGNMENT GUIDE WITH THUMB SCREWS | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
46 | 00885556710241 | E0015781-3 | E0015781-3 | SPIKED ELEVATOR - STRAIGHT | HTE | ELEVATOR | 1 | Peri-loc |
47 | 00885556708675 | E0015708-5 | E0015708-5 | GII PS TRIAL INSERT 5-6 9MM | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Legion |
48 | 00885556706978 | E0015771-1 | E0015771-1 | 2MM RECUT BLOCK | HWT | TEMPLATE | 1 | Legion |
49 | 00885556704561 | E0015694-2 | E0015694-2 | PATELLA DEPTH GAUGE - 5MM | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | Legion |
50 | 00885556704455 | E0015672-1 | E0015672-1 | JOURNEY CR FEMORAL IMPACTOR | JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Journey II |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00885556143117 | 71934292 | 71934292 | REFLECTION LINER XLPE 36 ID 20 DEG ANT +6 50-52 E | REFLECTION, MICROSTABLE | SMITH & NEPHEW, INC. |
2 | 00885556143100 | 71934293 | 71934293 | REFLECTION XLPE 40 20 DEG ANTEVERTED +4 58-60 G | REFLECTION, MICROSTABLE | SMITH & NEPHEW, INC. |
3 | 00885556143094 | 71934294 | 71934294 | REFLECTION LINER XLPE 40 ID 20 DEG ANT +4 62-64 H | REFLECTION, MICROSTABLE | SMITH & NEPHEW, INC. |
4 | 00885556143087 | 71934295 | 71934295 | TRIAL REFLECTION LINER XLPE 36 ID 20 DEG ANT +6 50-52 E | REFLECTION, MICROSTABLE | SMITH & NEPHEW, INC. |
5 | 00885556143070 | 71934296 | 71934296 | TRIAL REFLECTION LINER XLPE 40 ID 20 DEG ANT +4 58-60 G | REFLECTION, MICROSTABLE | SMITH & NEPHEW, INC. |
6 | 00885556143063 | 71934297 | 71934297 | TRIAL REFLECTION LINER XLPE 40 ID 20 DEG ANT +4 62-64 H | REFLECTION, MICROSTABLE | SMITH & NEPHEW, INC. |
7 | 00880304644571 | 904903P | 904903P | ALLthread PEEK-OPTIMA | BIOMET ORTHOPEDICS, LLC | |
8 | 00880304644564 | 904900P | 904900P | ALLthread PEEK-OPTIMA | BIOMET ORTHOPEDICS, LLC | |
9 | 00877972006343 | 360-010-001 | A Li Gator | GENICON, INC. | ||
10 | 00877972004578 | 350-000-104 | GeniClip | GENICON, INC. | ||
11 | 00877972004554 | 350-000-103 | GeniClip | GENICON, INC. | ||
12 | 00877972004530 | 350-000-102 | GeniClip | GENICON, INC. | ||
13 | 00877972004516 | 350-000-101 | GeniClip | GENICON, INC. | ||
14 | 00857774006000 | 100-200 | 100-200 | The Amsel Occluder Device is designed to easily and securely close blood vessels The Amsel Occluder Device is designed to easily and securely close blood vessels (veins or arteries as well as hollow ducts) during surgical procedures. It is intended for use in open general surgery procedures on tubular structures or blood vessels (arteries and veins) wherever a metal ligating clip is indicated and within the size range of 2.0mm to 7.0mm diameter. | Amsel Occluder Device | AMSEL MEDICAL CORPORATION |
15 | 00857596005007 | 20130 | 20130 | A sterile, metallic, non-bio-absorbable clasp designed to be implanted around a A sterile, metallic, non-bio-absorbable clasp designed to be implanted around a blood vessel, lymphatic vessel, other tubular anatomy, or a tissue bundle for permanent occlusion. It may be used for ligation in open and endoscopic (e.g., laparoscopic) surgeries. | Titanium Ligation Clip | VESOCCLUDE MEDICAL, LLC |
16 | 00841911101680 | MRM4008 | Biopsy Site Identifier | Mammotome MAMMOMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
17 | 00841911101673 | MRM4002 | Biopsy Site Identifier | Mammotome MAMMOMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
18 | 00841911101666 | MAM3014 | Biopsy Site Identifier | Mammotome CORMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
19 | 00841911101659 | MAM3008 | Biopsy Site Identifier | Mammotome MAMMOMARK 2 | DEVICOR MEDICAL PRODUCTS, INC. | |
20 | 00841911101642 | MAM3002 | Biopsy Site Identifier | Mammotome MAMMOMARK 2 | DEVICOR MEDICAL PRODUCTS, INC. | |
21 | 00841911101635 | MMK1001 | Biopsy Site Identifier | Mammotome revolve mammomark | DEVICOR MEDICAL PRODUCTS, INC. | |
22 | 00841911101628 | MMK1002 | Biopsy Site Identifier | Mammotome revolve MammoMark | DEVICOR MEDICAL PRODUCTS, INC. | |
23 | 00841911101611 | MMK1001 | Biopsy Site Identifier | Mammotome revolve MammoMark | DEVICOR MEDICAL PRODUCTS, INC. | |
24 | 00841911101604 | MMK0802 | Biopsy Site Identifier | Mammotome revolve MammoMark | DEVICOR MEDICAL PRODUCTS, INC. | |
25 | 00841911101598 | MAM3001 | Biopsy Site Identifier | Mammotome MAMMOMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
26 | 00841911101376 | MMK0801 | Biopsy Site Identifier | Mammotome revolve MammoMark | DEVICOR MEDICAL PRODUCTS, INC. | |
27 | 00841911100522 | MMK1003 | Biopsy Site Identifier | Mammotome revolve MammoMark | DEVICOR MEDICAL PRODUCTS, INC. | |
28 | 00841911100515 | MMK1002 | Biopsy Site Identifier | Mammotome revolve mammomark | DEVICOR MEDICAL PRODUCTS, INC. | |
29 | 00841911100492 | MMK0803 | Biopsy Site Identifier | Mammotome revolve MammoMark | DEVICOR MEDICAL PRODUCTS, INC. | |
30 | 00841911100485 | MMK0802 | Biopsy Site Identifier | Mammotome revolve mammomark | DEVICOR MEDICAL PRODUCTS, INC. | |
31 | 00841911100478 | MMK0801 | Biopsy Site Identifier | Mammotome revolve MammoMark | DEVICOR MEDICAL PRODUCTS, INC. | |
32 | 00841911100461 | MAM3015 | Biopsy Site Identifier | Mammotome CORMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
33 | 00841911100454 | MAM3014 | Biopsy Site Identifier | Mammotome CORMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
34 | 00841911100447 | MAM3008 | Biopsy Site Identifier | Mammotome MAMMOMARK 2 | DEVICOR MEDICAL PRODUCTS, INC. | |
35 | 00841911100430 | MAM3002 | Biopsy Site Identifier | Mammotome MAMMOMARK 2 | DEVICOR MEDICAL PRODUCTS, INC. | |
36 | 00841911100423 | MAM3001 | Biopsy Site Identifier | Mammotome MAMMOMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
37 | 00841911100416 | MRM4008 | Biopsy Site Identifier | Mammotome MAMMOMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
38 | 00841911100409 | MRM4002 | Biopsy Site Identifier | Mammotome MAMMOMARK | DEVICOR MEDICAL PRODUCTS, INC. | |
39 | 00840663109593 | 4008-08 | 4008-08 | AnastoClip GC 8cm (XLarge) | AnastoClip GC 8cm (XLarge) | LEMAITRE VASCULAR, INC. |
40 | 00840663109586 | 4008-07 | 4008-07 | AnastoClip GC 8cm (Large) | AnastoClip GC 8cm (Large) | LEMAITRE VASCULAR, INC. |
41 | 00840663109579 | 4008-06 | 4008-06 | AnastoClip GC 8cm (Medium) | AnastoClip GC 8cm (Medium) | LEMAITRE VASCULAR, INC. |
42 | 00840663109562 | 4008-05 | 4008-05 | AnastoClip GC 8cm (Small) | AnastoClip GC 8cm (Small) | LEMAITRE VASCULAR, INC. |
43 | 00840663102471 | 4007-08 | 4007-08 | Anastoclip GC Closure System, XL | Anastoclip GC Closure System | LEMAITRE VASCULAR, INC. |
44 | 00840663102464 | 4007-07 | 4007-07 | Anastoclip GC Closure System, Large | Anastoclip GC Closure System | LEMAITRE VASCULAR, INC. |
45 | 00840663102457 | 4007-06 | 4007-06 | Anastoclip GC Closure System, Medium (M) | Anastoclip GC Closure System | LEMAITRE VASCULAR, INC. |
46 | 00840663102396 | 4001-00 | 4001-00 | Anastoclip Universal Clip Remover, 6 pack | Anastoclip Universal Clip Remover | LEMAITRE VASCULAR, INC. |
47 | 00840663102389 | 4000-08 | 4000-08 | Anastoclip AC Closure System, XL | Anastoclip AC Closure System | LEMAITRE VASCULAR, INC. |
48 | 00840663102372 | 4000-07 | 4000-07 | Anastoclip AC Closure System, Large (L) | Anastoclip AC Closure System | LEMAITRE VASCULAR, INC. |
49 | 00840663102365 | 4000-06 | 4000-06 | Anastoclip AC Closure System, medium (M) | Anastoclip AC Closure System | LEMAITRE VASCULAR, INC. |
50 | 00840663102358 | 4000-05 | 4000-05 | Anastoclip AC Closure System, small (S) | Anastoclip AC Closure System | LEMAITRE VASCULAR, INC. |