No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00845694041133 | 395-4001-30 | 395-4001-30 | Tag, 0 Degree ExtremiFuse, 3.0 | HWC | Screw, fixation, bone | 2 | OsteoMed |
2 | 00845694041126 | 395-4001-24 | 395-4001-24 | Tag, 0 Degree ExtremiFuse, 2.4 | HWC | Screw, fixation, bone | 2 | OsteoMed |
3 | 00845694041119 | 395-4001-00 | 395-4001-00 | Tag, 0 Degree ExtremiFuse, Blank | HWC | Screw, fixation, bone | 2 | OsteoMed |
4 | 00845694041102 | 395-4000 | 395-4000 | ExtremiFuse Organizer Block | HWC | Screw, fixation, bone | 2 | OsteoMed |
5 | 00845694041096 | 395-2430 | 395-2430 | X-Ray Template, ExtremiFuse | HWC | Screw, fixation, bone | 2 | OsteoMed |
6 | 00845694041089 | 395-2200 | 395-2200 | ExtremiFuse Dual Cannulated Driver Handle | HWC | Screw, fixation, bone | 2 | OsteoMed |
7 | 00845694041072 | 395-2124 | 395-2124 | Broach, ExtremiFuse | HWC | Screw, fixation, bone | 2 | OsteoMed |
8 | 00845694041065 | 395-2027 | 395-2027 | Ø2.7mm Cannulated Drill, Quick Release | HWC | Screw, fixation, bone | 2 | OsteoMed |
9 | 00845694041058 | 395-2000 | 395-2000 | .035 x 3 K-Wire | HWC | Screw, fixation, bone | 2 | OsteoMed |
10 | 00845694041041 | 386-1705 | 386-1705 | Extraction System Tray | KWD | PROSTHESIS, TOE, HEMI-, PHALANGEAL | 2 | OsteoMed |
11 | 00845694041034 | 320-1029 | 320-1029 | Plate Bending Forceps, Large | HRS | Plate, fixation, bone | 2 | OsteoMed |
12 | 00845694041027 | 319-1030 | 319-1030 | 3.0mm x 10 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
13 | 00845694041010 | 319-1024 | 319-1024 | 2.4mm x 10 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
14 | 00845694041003 | 319-0030 | 319-0030 | 3.0mm x 0 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
15 | 00845694040990 | 319-0024 | 319-0024 | 2.4mm x 0 Degree ExtremiFuse Implant | HWC | Screw, fixation, bone | 2 | OsteoMed |
16 | 00845694040969 | 213-0127 | 213-0127 | 1.6mm, Left Zed Plate, 11mm | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
17 | 00845694040952 | 213-0126 | 213-0126 | 1.6mm, Right Zed Plate, 11mm | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
18 | 00845694040945 | 210-0255 | 210-0255 | 2.0mm Left L Plate, 23mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
19 | 00845694040938 | 210-0254 | 210-0254 | 2.0mm Right L Plate, 23mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
20 | 00845694040921 | 210-0253 | 210-0253 | 2.0mm Left L Plate, 18mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
21 | 00845694040914 | 210-0252 | 210-0252 | 2.0mm Right L Plate, 18mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
22 | 00845694040907 | 210-0251 | 210-0251 | 2.0mm Left L Plate, 15mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
23 | 00845694040891 | 210-0250 | 210-0250 | 2.0mm Right L Plate, 15mm, Rigid | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
24 | 00845694040884 | 211-1606-REV-G | 211-1606-REV-G | 1.6mm x 6mm AUTO-DRIVE Screw | HWC | Screw, fixation, bone | 2 | OsteoMed |
25 | 00845694040877 | 213-0018-SP | 213-0018-SP | 1.6mm Rigid Curved Plate, 10 Hole, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
26 | 00845694040860 | 212-0052-SP | 212-0052-SP | 19mm T Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
27 | 00845694040853 | 212-0046-SP | 212-0046-SP | 13mm Right L Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
28 | 00845694040846 | 212-0044-SP | 212-0044-SP | 13mm Left L Plate, Sterile | JEY | PLATE, BONE | 2 | OsteoMed |
29 | 00845694040839 | 212-0030-SP | 212-0030-SP | 7 Hole Y Plate, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
30 | 00845694040822 | 213-0011-SP | 213-0011-SP | 10 Hole Curved Plate, Sterile | DZL | SCREW, FIXATION, INTRAOSSEOUS | 2 | OsteoMed |
31 | 00845694040815 | 817-1017 | 817-1017 | PrimaLIF LLIF 17mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
32 | 00845694040808 | 817-1015 | 817-1015 | PrimaLIF LLIF 15mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
33 | 00845694040792 | 817-1013 | 817-1013 | PrimaLIF LLIF 13mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
34 | 00845694040785 | 817-1011 | 817-1011 | PrimaLIF LLIF 11mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
35 | 00845694040778 | 817-1009 | 817-1009 | PrimaLIF LLIF 9mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
36 | 00845694040761 | 817-1007 | 817-1007 | PrimaLIF LLIF 7mm x 26mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
37 | 00845694040754 | 816-1017 | 816-1017 | PrimaLIF LLIF 17mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
38 | 00845694040747 | 816-1015 | 816-1015 | PrimaLIF LLIF 15mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
39 | 00845694040730 | 816-1013 | 816-1013 | PrimaLIF LLIF 13mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
40 | 00845694040723 | 816-1011 | 816-1011 | PrimaLIF LLIF 11mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
41 | 00845694040716 | 816-1009 | 816-1009 | PrimaLIF LLIF 9mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
42 | 00845694040709 | 816-1007 | 816-1007 | PrimaLIF LLIF 7mm x 22mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
43 | 00845694040693 | 815-1017 | 815-1017 | PrimaLIF LLIF 17mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
44 | 00845694040686 | 815-1015 | 815-1015 | PrimaLIF LLIF 15mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
45 | 00845694040679 | 815-1013 | 815-1013 | PrimaLIF LLIF 13mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
46 | 00845694040662 | 815-1011 | 815-1011 | PrimaLIF LLIF 11mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
47 | 00845694040655 | 815-1009 | 815-1009 | PrimaLIF LLIF 9mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
48 | 00845694040648 | 815-1007 | 815-1007 | PrimaLIF LLIF 7mm x 18mm Lordotic Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
49 | 00845694040631 | 814-1017 | 814-1017 | PrimaLIF LLIF 17mm x 26mm Parallel Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
50 | 00845694040624 | 814-1015 | 814-1015 | PrimaLIF LLIF 15mm x 26mm Parallel Trial | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | OsteoMed |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 09120034303678 | 65394 | 65394 | Bolt Cutter, Pelvis Screws, Sacral Rod | Bolt Cutter | I.T.S. GMBH |
2 | 08809399746191 | IOC-041 | Mesh cutter | Neuro Plating System | OSTEONIC CO.,LTD. | |
3 | 08809399746184 | IOC-040 | Plate cutter | Neuro Plating System | OSTEONIC CO.,LTD. | |
4 | 08800037569806 | PL0420 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
5 | 08800037569790 | PL0410 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
6 | 08800037569783 | PL0400 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
7 | 08800037569721 | OS0120 | ANAX™ OCT SPINAL SYSTEM | U&I CORPORATION | ||
8 | 08800037546050 | SF0390 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
9 | 08800037546043 | SF0140 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
10 | 08800037545794 | PLS0300 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
11 | 08800037545787 | PLS0290 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
12 | 08800037544711 | PLS0280 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
13 | 08800037542779 | SF0390 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
14 | 08800037527714 | PLS0240 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
15 | 08800037527707 | PLS0230 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
16 | 08800037527691 | PLS0220 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
17 | 08800037527684 | PLS0210 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
18 | 08800037527677 | PLS0200 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
19 | 08800037507839 | TLS1005 | Velofix™ TLIF Cage | U&I CORPORATION | ||
20 | 08800037507822 | TLS1004 | Velofix™ TLIF Cage | U&I CORPORATION | ||
21 | 08800037507815 | TLS1003 | Velofix™ TLIF Cage | U&I CORPORATION | ||
22 | 08800037507808 | TLS1002 | Velofix™ TLIF Cage | U&I CORPORATION | ||
23 | 08800037507792 | TLS1001 | Velofix™ TLIF Cage | U&I CORPORATION | ||
24 | 08800015995443 | TL0420 | Velofix™ TLIF Cage | U&I CORPORATION | ||
25 | 08800015995436 | TL0410 | Velofix™ TLIF Cage | U&I CORPORATION | ||
26 | 08800015995429 | TL0400 | Velofix™ TLIF Cage | U&I CORPORATION | ||
27 | 08800015956277 | PLS0150 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
28 | 08800015956260 | PLS0140 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
29 | 08800015956253 | PLS0130 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
30 | 08800015954709 | PL0420 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
31 | 08800015954693 | PL0410 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
32 | 08800015954686 | PL0400 | Velofix™ PEEK Lumbar Cage | U&I CORPORATION | ||
33 | 08800015954020 | PE1040 | VELOFIX™ PEEK CERVICAL CAGE | U&I CORPORATION | ||
34 | 08800015952071 | SP0019 | Optima™ Spinal System | U&I CORPORATION | ||
35 | 08800015950961 | OS0120 | ANAX™ OCT System | U&I CORPORATION | ||
36 | 08800015948142 | SND0190 | PERFIX DEFORMITY INSTRUMENT SYSTEM | U&I CORPORATION | ||
37 | 08800015947701 | SS0190 | Perfix™ MIS | U&I CORPORATION | ||
38 | 08800015947695 | SS0180 | Perfix™ MIS | U&I CORPORATION | ||
39 | 08800015946513 | SGS1002 | Global Spinal Fixation System™ | U&I CORPORATION | ||
40 | 07898506814084 | QO.222.01 | QO.222.01 | Torquing and bending macho pliers | Quinelato | SCHOBELL INDUSTRIAL LTDA |
41 | 06438408007255 | 1 | INS-9618 | Suture cutter | Inion® Shoulder Instrumentation | INION OY |
42 | 06438408004063 | 1 | IFS-9051 | Screw cutting pliers (INS-9109) | Inion FreedomScrew instruments | INION OY |
43 | 06438408002069 | 1 | INS-9109 | Screw cutting pliers | Inion® Universal instruments | INION OY |
44 | 05033955114206 | LANCE STITCH CUTTERS | L420 | Suture cutter. A dedicated hand held surgical instrument used for cutting suture Suture cutter. A dedicated hand held surgical instrument used for cutting sutures. It will typically have a protected scalpel like blade which may be fixed or have a scissor cutting action. | Swann Morton Ltd. | SWANN-MORTON LIMITED |
45 | 05033955104207 | PARAGON STITCH CUTTER | P420 | Suture cutter. A dedicated hand held surgical instrument used for cutting suture Suture cutter. A dedicated hand held surgical instrument used for cutting sutures. It will typically have a protected scalpel like blade which may be fixed or have a scissor cutting action. | Swann Morton Ltd. | SWANN-MORTON LIMITED |
46 | 05033955049263 | STITCH CUTTER STERILE RETRACTABLE SCALPELS | 4926 | Suture cutter, reusable. A dedicated hand-held surgical instrument designed for Suture cutter, reusable. A dedicated hand-held surgical instrument designed for cutting sutures. It will typically have a protected scalpel-like blade which may be fixed or have a scissors-like cutting action. This is a reusable device. | Swann Morton Ltd. | SWANN-MORTON LIMITED |
47 | 05033955040260 | STITCH CUTTER BULK NON STERILE RETRACTABLE SCALPELS | 4026 | Suture cutter, reusable. A dedicated hand-held surgical instrument designed for Suture cutter, reusable. A dedicated hand-held surgical instrument designed for cutting sutures. It will typically have a protected scalpel-like blade which may be fixed or have a scissors-like cutting action. This is a reusable device. | Swann Morton Ltd. | SWANN-MORTON LIMITED |
48 | 05033955039264 | STITCH CUTTER STERILE RETRACTABLE SCALPEL | 3926 | Suture cutter, reusable. A dedicated hand-held surgical instrument designed for Suture cutter, reusable. A dedicated hand-held surgical instrument designed for cutting sutures. It will typically have a protected scalpel-like blade which may be fixed or have a scissors-like cutting action. This is a reusable device. | Swann Morton Ltd. | SWANN-MORTON LIMITED |
49 | 05033955019617 | CMI BULK No. 3 STAINLESS STITCH CUTTERS (BRAND) | 1961 | Suture cutter. A dedicated hand held surgical instrument used for cutting suture Suture cutter. A dedicated hand held surgical instrument used for cutting sutures. It will typically have a protected scalpel like blade which may be fixed or have a scissor cutting action. | Swann Morton Ltd. | SWANN-MORTON LIMITED |
50 | 05033955019600 | BULK No. 3 STAINLESS STITCH CUTTERS | 1960 | Suture cutter. A dedicated hand held surgical instrument used for cutting suture Suture cutter. A dedicated hand held surgical instrument used for cutting sutures. It will typically have a protected scalpel like blade which may be fixed or have a scissor cutting action. | Swann Morton Ltd. | SWANN-MORTON LIMITED |