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 | 07613327338614 | I-K3833TS29 | I-K3833TS29 | SPECIALTY TRIATHLON TIBIAL STYLUS | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
2 | 07613327330700 | I-K2871TS29 | I-K2871TS29 | SPECIALTY TRIATHLON PKR TIBIAL STYLUS SIZE 2 AND 9mm | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
3 | 07613327319064 | I-K1852TS27 | I-K1852TS27 | SPECIALTY TRIATHLON TIBIAL STYLUS 2MM AND 7MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
4 | 07613327318968 | I-K1852TS35 | I-K1852TS35 | SPECIALTY TRIATHLON TIBIAL STYLUS 3MM AND 5MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
5 | 07613327318807 | I-K2084T411 | I-K2084T411 | SPECIALTY TRIATHLON TIBIAL STYLUS 4MM AND 11MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
6 | 07613327318784 | I-K1852TS14 | I-K1852TS14 | SPECIALTY TRIATHLON TIBIAL STYLUS 1MM AND 4MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
7 | 07613327318678 | I-K1852TS09 | I-K1852TS09 | SPECIALTY TRIATHLON TIBIAL STYLUS 0MM AND 9MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
8 | 07613327318661 | I-K1852TS28 | I-K1852TS28 | SPECIALTY TRIATHLON TIBIAL STYLUS 2MM AND 8MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
9 | 07613327318487 | I-K1852TS24 | I-K1852TS24 | SPECIALTY TRIATHLON TIBIAL STYLUS 2MM AND 4MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
10 | 07613327318463 | I-K1852TS41 | I-K1852TS41 | SPECIALTY TRIATHLON TIBIAL STYLUS 4MM AND 10MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
11 | 07613327318449 | I-K1852TS21 | I-K1852TS21 | SPECIALTY TRIATHLON TIBIAL STYLUS 2MM AND 11MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
12 | 07613327318340 | I-K18520006 | I-K18520006 | SPECIALTY TRIATHLON TIBIAL STYLUS 0MM AND 6MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
13 | 07613327318319 | I-K2084TS29 | I-K2084TS29 | SPECIALTY TRIATHLON TIBIAL STYLUS 2MM AND 9MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
14 | 07613327318258 | I-K1852T411 | I-K1852T411 | SPECIALTY TRIATHLON TIBIAL STYLUS 4MM AND 11MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
15 | 07613327318241 | I-K18521113 | I-K18521113 | SPECIALTY TRIATHLON TIBIAL STYLUS 11MM AND 13MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
16 | 07613327317923 | I-K1852TS02 | I-K1852TS02 | SPECIALTY TRIATHLON TIBIAL STYLUS 10MM AND 12MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
17 | 07613327317770 | I-K18520004 | I-K18520004 | SPECIALTY TRIATHLON TIBIAL STYLUS 0MM AND 4MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
18 | 07613327317381 | I-K1852TS62 | I-K1852TS62 | SPECIALTY TRIATHLON TIBIAL STYLUS 2MM AND 6MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
19 | 07613327317282 | I-K1852TS79 | I-K1852TS79 | SPECIALTY TRIATHLON TIBIAL STYLUS 7MM AND 9MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
20 | 07613327317206 | I-K1852TS57 | I-K1852TS57 | SPECIALTY TRIATHLON TIBIAL STYLUS 5MM AND 7MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
21 | 07613327317183 | I-K1852TS47 | I-K1852TS47 | SPECIALTY TRIATHLON TIBIAL STYLUS 4MM AND 7MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
22 | 07613327317114 | I-K1852TS49 | I-K1852TS49 | SPECIALTY TRIATHLON TIBIAL STYLUS 4MM AND 9MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
23 | 07613327317046 | I-K1852TS46 | I-K1852TS46 | SPECIALTY TRIATHLON TIBIAL STYLUS 4MM AND 6MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
24 | 07613327317008 | I-K1852TS56 | I-K1852TS56 | SPECIALTY TRIATHLON TIBIAL STYLUS 5MM AND 6MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
25 | 07613327316193 | I-K3498TS00 | I-K3498TS00 | SPECIALTY TRIATHLON MIS TIBIAL STYLUS 2MM AND 9MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
26 | 07613327297133 | I-K3119AS00 | I-K3119AS00 | SPECIALTY TRIATHLON ADJUSTABLE TIBIAL STYLUS | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
27 | 07613327247046 | 6543-2-601 | 6543-2-601 | TIBIAL OFFSET BUSHING GUIDE TRIATHLON REVISION INSTRUMENTS | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
28 | 07613327234213 | 8000-0209 | 8000-0209 | TIBIAL STYLUS 2/9MM | INSTRUMENT | HOWMEDICA OSTEONICS CORP. |
29 | 07613327056327 | 0242010300 | 0242-010-300 | Mini Small-Joint Grasper | NA | STRYKER CORPORATION |
30 | 07613327056310 | 0242010400 | 0242-010-400 | Mini Small-Joint Scissors | NA | STRYKER CORPORATION |
31 | 07613327056303 | 0242010200 | 0242-010-200 | Mini Small-Joint Punch | NA | STRYKER CORPORATION |
32 | 07332339203863 | 105-16811 | 105-16811 | BONE CUTTING FORCEPS ORIGINAL STILLE curved 19 cm 7.5 in | STILLE Bone Cutters | STILLE AB |
33 | 07332339203856 | 105-16512 | 105-16512 | BONE CUTTING FORCEPS STILLE angled 18 cm 7 in | STILLE Bone Cutters | STILLE AB |
34 | 07332339203849 | 105-16510 | 105-16510 | BONE CUTTING FORCEPS STILLE straight 17 cm 6.75 in | STILLE Bone Cutters | STILLE AB |
35 | 05019279431861 | 32-422939 | 32-422939 | Oxford® Partial Knee SystemOsteophyte Removal Tool | BIOMET UK LTD | |
36 | 05019279431847 | 32-422938 | 32-422938 | Oxford® Partial Knee SystemOsteophyte Removal Tool | BIOMET UK LTD | |
37 | 05019279426478 | 32-422937 | 32-422937 | Oxford Partial Knee SystemOsteophyte Tool | BIOMET UK LTD | |
38 | 05019279426430 | 32-422935 | 32-422935 | Oxford Partial Knee SystemOsteophyte Tool | BIOMET UK LTD | |
39 | 05019279124237 | 32-422344 | 32-422344 | OXFORD UNICOMPARTMENTAL KNEE PHASE 3POSTERIOR OSTEOPHYTE CHISEL | BIOMET UK LTD | |
40 | 05019279068692 | 31-600386 | 31-600386 | RECAP/MAGNUM HIP INSTRUMENTATION | BIOMET UK LTD | |
41 | 04050435041129 | 27-08340 | 27-08340 | Plate Cutting Forceps M3 | MONDEAL | MONDEAL MEDICAL SYSTEMS GMBH |
42 | 04050435040887 | 27-08120 | 27-08120 | Plate Cutting Forceps M1/M2 | MONDEAL | MONDEAL MEDICAL SYSTEMS GMBH |
43 | 04046964253553 | NS407R | NS407R | IQ MEDIALIZED TIBIA CUTTING GUIDE RIGHT | COLUMBUS REVISION | AESCULAP AG |
44 | 04046964253546 | NS406R | NS406R | IQ MEDIALIZED TIBIA CUTTING GUIDE LEFT | COLUMBUS REVISION | AESCULAP AG |
45 | 04046964158735 | NQ1041R | NQ1041R | IQ COLUMBUS 4-IN-1 FEM.CUTTING GUIDE F1 | IQ COLUMBUS | AESCULAP AG |
46 | 04046964158728 | NQ1042R | NQ1042R | IQ COLUMBUS 4-IN-1 FEM.CUTTING GUIDE F2 | IQ COLUMBUS | AESCULAP AG |
47 | 04046964158711 | NQ1046R | NQ1046R | IQ COLUMBUS 4-IN-1 FEM.CUTTING GUIDE F6 | IQ COLUMBUS | AESCULAP AG |
48 | 04046964158704 | NQ1047R | NQ1047R | IQ COLUMBUS 4-IN-1 FEM.CUTTING GUIDE F7 | IQ COLUMBUS | AESCULAP AG |
49 | 04046964158599 | NQ1048R | NQ1048R | IQ COLUMBUS 4-IN-1 FEM.CUTTING GUIDE F8 | IQ COLUMBUS | AESCULAP AG |
50 | 04046964156816 | NQ1043R | NQ1043R | IQ COLUMBUS 4-IN-1 FEM.CUTTING GUIDE F3 | IQ COLUMBUS | AESCULAP AG |