No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | M711CRT006ST0 | CRT006ST | CP Ti | GWO | Plate, Cranioplasty, Preformed, Alterable | 2 | Neuro & Craniofacial Fixation System | |
2 | M711E20024 | E2002 | E2002 | KWQ,KWP,MNH,MNI,NKB | Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | Excella II® | ||
3 | M711BTA1190 | BTA-119 | Al, SST, Nylon, Silicone | LXH | Orthopedic Manual Surgical Instrument | 1 | PSO | |
4 | M711X212163200 | X21216320 | X21216320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
5 | M711X212163000 | X21216300 | X21216300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
6 | M711X212162800 | X21216280 | X21216280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
7 | M711X212153200 | X21215320 | X21215320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
8 | M711X212153000 | X21215300 | X21215300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
9 | M711X212152800 | X21215280 | X21215280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
10 | M711X212143200 | X21214320 | X21214320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
11 | M711X212143000 | X21214300 | X21214300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
12 | M711X212142800 | X21214280 | X21214280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
13 | M711X212133200 | X21213320 | X21213320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
14 | M711X212133000 | X21213300 | X21213300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
15 | M711X212132800 | X21213280 | X21213280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
16 | M711X212123200 | X21212320 | X21212320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
17 | M711X212123000 | X21212300 | X21212300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
18 | M711X212122800 | X21212280 | X21212280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
19 | M711X212113200 | X21211320 | X21211320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
20 | M711X212113000 | X21211300 | X21211300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
21 | M711X212112800 | X21211280 | X21211280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
22 | M711X212103200 | X21210320 | X21210320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
23 | M711X212103000 | X21210300 | X21210300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
24 | M711X212102800 | X21210280 | X21210280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
25 | M711X212093200 | X21209320 | X21209320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
26 | M711X212093000 | X21209300 | X21209300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
27 | M711X212092800 | X21209280 | X21209280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
28 | M711X212082800 | X21208280 | X21208280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
29 | M711X210162550 | X21016255 | X21016255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
30 | M711X210162500 | X21016250 | X21016250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
31 | M711X210162250 | X21016225 | X21016225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
32 | M711X210162200 | X21016220 | X21016220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
33 | M711X210153200 | X21015320 | X21015320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
34 | M711X210152800 | X21015280 | X21015280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
35 | M711X210152550 | X21015255 | X21015255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
36 | M711X210152500 | X21015250 | X21015250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
37 | M711X210152250 | X21015225 | X21015225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
38 | M711X210152200 | X21015220 | X21015220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
39 | M711X210143200 | X21014320 | X21014320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
40 | M711X210142800 | X21014280 | X21014280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
41 | M711X210142550 | X21014255 | X21014255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
42 | M711X210142500 | X21014250 | X21014250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
43 | M711X210142250 | X21014225 | X21014225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
44 | M711X210142200 | X21014220 | X21014220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
45 | M711X210133200 | X21013320 | X21013320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
46 | M711X210132800 | X21013280 | X21013280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
47 | M711X210132550 | X21013255 | X21013255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
48 | M711X210132500 | X21013250 | X21013250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
49 | M711X210132250 | X21013225 | X21013225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
50 | M711X210132200 | X21013220 | X21013220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 03596010486912 | 71063016 | 71063016 | 5MM SHORT TISSUE PROTECTOR | Jet-X | SMITH & NEPHEW, INC. |
2 | 03596010486509 | 71053030 | 71053030 | CENTRAL BODY BOLT 8MM | OTHER EXTERNAL FIXATION | SMITH & NEPHEW, INC. |
3 | 03596010484956 | 71430441 | 71430441 | GENESIS II OVAL RESURFACING PATELLAR TRIAL 41MM | GENESIS II | SMITH & NEPHEW, INC. |
4 | 03596010484932 | 71430435 | 71430435 | GENESIS II OVAL RESURFACING PATELLAR TRIAL 35MM | GENESIS II | SMITH & NEPHEW, INC. |
5 | 03596010484925 | 71430432 | 71430432 | GENESIS II OVAL RESURFACING PATELLAR TRIAL 32MM | GENESIS II | SMITH & NEPHEW, INC. |
6 | 03596010484918 | 71430429 | 71430429 | GENESIS II OVAL RESURFACING PATELLAR TRIAL 29MM | GENESIS II | SMITH & NEPHEW, INC. |
7 | 03596010484307 | 7210285 | 7210285 | MTO ACUFEX ACL AMR LEFT KNEE | ACUFEX | SMITH & NEPHEW, INC. |
8 | 03596010484284 | 7210286 | 7210286 | MTO ACUFEX ACL AMR RGHT KNEE | ACUFEX | SMITH & NEPHEW, INC. |
9 | 03596010484123 | 71441161 | 71441161 | GENESIS II MINAMALLY INVASIVE DISTAL FEMORAL STYLUS | GENESIS II | SMITH & NEPHEW, INC. |
10 | 03596010484062 | 71441134 | 71441134 | GII MIN INV HOUSING RESECTION BLOCK SZ 8 | GENESIS II | SMITH & NEPHEW, INC. |
11 | 03596010484055 | 71441133 | 71441133 | GII MIN INV HOUSING RESECTION BLOCK SZ 7 | GENESIS II | SMITH & NEPHEW, INC. |
12 | 03596010484048 | 71441132 | 71441132 | GENESIS II MINAMALLY INVASIVE HOUSING RESECTI GENESIS II MINAMALLY INVASIVE HOUSING RESECTION BLOCK SIZE 6 | GENESIS II | SMITH & NEPHEW, INC. |
13 | 03596010484031 | 71441131 | 71441131 | GII MIN INV HOUSING RESECTION BLOCK SZ 5 | GENESIS II | SMITH & NEPHEW, INC. |
14 | 03596010484024 | 71441130 | 71441130 | GENESIS II MINAMALLY INVASIVE HOUSING RESECTI GENESIS II MINAMALLY INVASIVE HOUSING RESECTION BLOCK SIZE 4 | GENESIS II | SMITH & NEPHEW, INC. |
15 | 03596010484017 | 71441129 | 71441129 | GENESIS II MINAMALLY INVASIVE HOUSING RESECTI GENESIS II MINAMALLY INVASIVE HOUSING RESECTION BLOCK SIZE 3 | GENESIS II | SMITH & NEPHEW, INC. |
16 | 03596010484000 | 71441128 | 71441128 | GENESIS II MINAMALLY INVASIVE HOUSING RESECTI GENESIS II MINAMALLY INVASIVE HOUSING RESECTION BLOCK SIZE 2 | GENESIS II | SMITH & NEPHEW, INC. |
17 | 03596010483997 | 71441127 | 71441127 | GII MIN INV HOUSING RESECTION BLOCK SZ 1 | GENESIS II | SMITH & NEPHEW, INC. |
18 | 03596010483621 | 71249865 | 71249865 | HUMERAL COMMA GUIDE | COFIELD | SMITH & NEPHEW, INC. |
19 | 03596010482860 | 71364033 | 71364033 | MINIMAL INCISION WIDE HOHMAN BENT RETRACTOR | NA | SMITH & NEPHEW, INC. |
20 | 03596010482853 | 71364032 | 71364032 | MINIMAL INCISION NARROW HOHMAN BENT RETRACTOR | NA | SMITH & NEPHEW, INC. |
21 | 03596010481771 | 71367912 | 71367912 | TANDEM UNIPOLAR CONVERSION TRIAL +12MM | TANDEM | SMITH & NEPHEW, INC. |
22 | 03596010481764 | 71367908 | 71367908 | TANDEM UNIPOLAR CONVERSION TRIAL +8MM | TANDEM | SMITH & NEPHEW, INC. |
23 | 03596010481757 | 71367904 | 71367904 | TANDEM UNIPOLAR CONVERSION TRIAL +4MM | TANDEM | SMITH & NEPHEW, INC. |
24 | 03596010481740 | 71367903 | 71367903 | TANDEM UNIPOLAR CONVERSION TRIAL -3MM | TANDEM | SMITH & NEPHEW, INC. |
25 | 03596010481733 | 71367900 | 71367900 | TANDEM UNIPOLAR CONVERSION TRIAL 0MM | TANDEM | SMITH & NEPHEW, INC. |
26 | 03596010481702 | 71363059 | 71363059 | TANDEM TRIAL SHELL 59MM | TANDEM | SMITH & NEPHEW, INC. |
27 | 03596010481696 | 71363057 | 71363057 | TANDEM TRIAL SHELL 57MM | TANDEM | SMITH & NEPHEW, INC. |
28 | 03596010481689 | 71363055 | 71363055 | TANDEM TRIAL SHELL 55MM | TANDEM | SMITH & NEPHEW, INC. |
29 | 03596010481672 | 71363054 | 71363054 | TANDEM TRIAL SHELL 54MM | TANDEM | SMITH & NEPHEW, INC. |
30 | 03596010481665 | 71363053 | 71363053 | TANDEM TRIAL SHELL 53MM | TANDEM | SMITH & NEPHEW, INC. |
31 | 03596010481658 | 71363052 | 71363052 | TANDEM TRIAL SHELL 52MM | TANDEM | SMITH & NEPHEW, INC. |
32 | 03596010481641 | 71363051 | 71363051 | TANDEM TRIAL SHELL 51MM | TANDEM | SMITH & NEPHEW, INC. |
33 | 03596010481634 | 71363050 | 71363050 | TANDEM TRIAL SHELL 50MM | TANDEM | SMITH & NEPHEW, INC. |
34 | 03596010481627 | 71363049 | 71363049 | TANDEM TRIAL SHELL 49MM | TANDEM | SMITH & NEPHEW, INC. |
35 | 03596010481610 | 71363048 | 71363048 | TANDEM TRIAL SHELL 48MM | TANDEM | SMITH & NEPHEW, INC. |
36 | 03596010481603 | 71363047 | 71363047 | TANDEM TRIAL SHELL 47MM | TANDEM | SMITH & NEPHEW, INC. |
37 | 03596010481597 | 71363046 | 71363046 | TANDEM TRIAL SHELL 46MM | TANDEM | SMITH & NEPHEW, INC. |
38 | 03596010481580 | 71363045 | 71363045 | TANDEM TRIAL SHELL 45MM | TANDEM | SMITH & NEPHEW, INC. |
39 | 03596010481573 | 71363044 | 71363044 | TANDEM TRIAL SHELL 44MM | TANDEM | SMITH & NEPHEW, INC. |
40 | 03596010481566 | 71363043 | 71363043 | TANDEM TRIAL SHELL 43MM | TANDEM | SMITH & NEPHEW, INC. |
41 | 03596010481559 | 71363042 | 71363042 | TANDEM TRIAL SHELL 42MM | TANDEM | SMITH & NEPHEW, INC. |
42 | 03596010481542 | 71363041 | 71363041 | TANDEM TRIAL SHELL 41MM | TANDEM | SMITH & NEPHEW, INC. |
43 | 03596010481535 | 71363040 | 71363040 | TANDEM TRIAL SHELL 40MM | TANDEM | SMITH & NEPHEW, INC. |
44 | 03596010481436 | 71430356 | 71430356 | GENESIS II ARTICULAR INSERT SPACER TRIAL SIZE 1-2 25MM | GENESIS II | SMITH & NEPHEW, INC. |
45 | 03596010481412 | 71430324 | 71430324 | GENESIS II ARTICULAR INSERT SPACER TRIAL SIZE 1-2 13MM | GENESIS II | SMITH & NEPHEW, INC. |
46 | 03596010481399 | 71430962 | 71430962 | GII CONSTRAINED ARTICULAR TRIAL SZ 1-2 11MM | GENESIS II | SMITH & NEPHEW, INC. |
47 | 03596010481382 | 71430961 | 71430961 | GENESIS II CONSTRAINED ARTICULAR TRIAL SIZE 1-2 9MM | GENESIS II | SMITH & NEPHEW, INC. |
48 | 03596010481375 | 71430903 | 71430903 | GENESIS II POSTERIOR STABILIZING ARTICULAR TR GENESIS II POSTERIOR STABILIZING ARTICULAR TRIAL SIZE 1-2 11MM | GENESIS II | SMITH & NEPHEW, INC. |
49 | 03596010481368 | 71430901 | 71430901 | GENESIS II POSTERIOR STABILIZING ARTICULAR TR GENESIS II POSTERIOR STABILIZING ARTICULAR TRIAL SIZE 1-2 9MM | GENESIS II | SMITH & NEPHEW, INC. |
50 | 03596010481351 | 71430456 | 71430456 | GENESIS II DISHED ARTICULAR TRIAL SIZE 1-2 11MM | GENESIS II | SMITH & NEPHEW, INC. |