No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00889024464315 | 00-7050-078-00 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | NA | ||
2 | 00889024464292 | 00-7050-076-00 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | NA | ||
3 | 00889024464278 | 00-7050-038-00 | HWR | DRIVER, PROSTHESIS | 1 | NA | ||
4 | 00889024464261 | 00-7050-036-00 | HWR | DRIVER, PROSTHESIS | 1 | NA | ||
5 | 00889024464254 | 00-7361-052-22 | HXB | PROBE | 1 | NA | ||
6 | 00889024464247 | 00-7360-070-28 | HXB | PROBE | 1 | NA | ||
7 | 00889024464230 | 00-7360-068-28 | HXB | PROBE | 1 | NA | ||
8 | 00889024464223 | 00-7360-066-28 | HXB | PROBE | 1 | NA | ||
9 | 00889024464216 | 00-7360-064-28 | HXB | PROBE | 1 | NA | ||
10 | 00889024464209 | 00-7360-062-28 | HXB | PROBE | 1 | NA | ||
11 | 00889024464193 | 00-7360-060-28 | HXB | PROBE | 1 | NA | ||
12 | 00889024464186 | 00-7360-058-28 | HXB | PROBE | 1 | NA | ||
13 | 00889024464179 | 00-7360-056-28 | HXB | PROBE | 1 | NA | ||
14 | 00889024464162 | 00-7360-054-28 | HXB | PROBE | 1 | NA | ||
15 | 00889024464155 | 00-7360-052-28 | HXB | PROBE | 1 | NA | ||
16 | 00889024320635 | 96-701-30001 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | ||
17 | 00889024320628 | 96-701-21161 | 96-701-21161 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | |
18 | 00889024320611 | 96-701-21121 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | ||
19 | 00889024320604 | 96-701-21101 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | ||
20 | 00889024320598 | 96-701-21081 | 96-701-21081 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | |
21 | 00889024320581 | 96-701-20161 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | ||
22 | 00889024320574 | 96-701-20121 | 96-701-20121 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | |
23 | 00889024320567 | 96-701-20101 | 96-701-20101 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | |
24 | 00889024320550 | 96-701-20081 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | ||
25 | 00889024320543 | 96-701-10001 | 96-701-10001 | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | TM Ardis® | |
26 | 00889024320536 | 96-499-60001 | 96-499-60001 | FSM,MQP,MAX | TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebr TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar | 1 | NA | |
27 | 00889024320529 | 96-499-50001 | 96-499-50001 | MQP,MAX,FSM | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT | 1 | NA | |
28 | 00889024320512 | 96-499-40001 | 96-499-40001 | MQP,MAX,FSM | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT | 1 | NA | |
29 | 00889024320505 | 96-499-30001 | 96-499-30001 | MAX,MQP,FSM | Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT | 1 | NA | |
30 | 00889024320499 | 96-499-20001 | 96-499-20001 | MQP,MAX,FSM | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT | 1 | NA | |
31 | 00889024320482 | 96-499-10001 | 96-499-10001 | MQP,FSM,MAX | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebr SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebral fusion device with bone graft, lumbar | 1 | NA | |
32 | 00889024320031 | 96-215-21031 | 96-215-21031 | GAD | RETRACTOR | 1 | NA | |
33 | 00889024320024 | 96-215-21021 | 96-215-21021 | GAD | RETRACTOR | 1 | NA | |
34 | 00889024320017 | 96-215-21011 | 96-215-21011 | GAD | RETRACTOR | 1 | NA | |
35 | 00889024320000 | 96-215-21001 | 96-215-21001 | GAD | RETRACTOR | 1 | NA | |
36 | 00889024319998 | 96-215-20001 | 96-215-20001 | GAD | RETRACTOR | 1 | NA | |
37 | 00889024319981 | 96-215-19011 | 96-215-19011 | GAD | RETRACTOR | 1 | NA | |
38 | 00889024319974 | 96-215-19001 | 96-215-19001 | GAD | RETRACTOR | 1 | NA | |
39 | 00889024319967 | 96-215-18001 | 96-215-18001 | GAD | RETRACTOR | 1 | NA | |
40 | 00889024319950 | 96-215-17011 | 96-215-17011 | GAD | RETRACTOR | 1 | NA | |
41 | 00889024319943 | 96-215-17001 | 96-215-17001 | GAD | RETRACTOR | 1 | NA | |
42 | 00889024319936 | 96-215-16001 | 96-215-16001 | GAD | RETRACTOR | 1 | NA | |
43 | 00889024319929 | 96-215-15011 | 96-215-15011 | GAD | RETRACTOR | 1 | NA | |
44 | 00889024319912 | 96-215-15001 | 96-215-15001 | GAD | RETRACTOR | 1 | NA | |
45 | 00889024319905 | 96-215-14011 | 96-215-14011 | GAD | RETRACTOR | 1 | NA | |
46 | 00889024319899 | 96-215-14001 | 96-215-14001 | GAD | RETRACTOR | 1 | NA | |
47 | 00889024319882 | 96-215-13011 | 96-215-13011 | GAD | RETRACTOR | 1 | NA | |
48 | 00889024319875 | 96-215-13001 | 96-215-13001 | GAD | RETRACTOR | 1 | NA | |
49 | 00889024319868 | 96-215-12011 | 96-215-12011 | GAD | RETRACTOR | 1 | NA | |
50 | 00889024319851 | 96-215-12001 | 96-215-12001 | GAD | RETRACTOR | 1 | NA |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 10603295523833 | 4862-00-050 | 486200050 | CANAL PROBE CURVED | NA | DEPUY (IRELAND) |
2 | 10603295515685 | 4862-00-040 | 486200040 | CANAL PROBE STRAIGHT | NA | DEPUY (IRELAND) |
3 | 10603295325239 | L94018 | L94018 | CANAL EXPLORER | NA | DEPUY (IRELAND) |
4 | 10603295223597 | 9400-80-001 | 940080001 | PROXIMA CANAL FINDER | NA | DEPUY INTERNATIONAL LTD |
5 | 10381780466765 | 225133 | 225-133 | Bunnel Dissecting Probe, 5", 1.5mm Tip Diameter | Integra® Jarit® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
6 | 10381780461630 | 840320 | 840-320 | Probe and Packer, 6", Blunt Probe and 2mm x 25mm Packer | Integra® Jarit® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
7 | 10381780460619 | PM-4739HK | PM-4739HK | Worst Pigtail Probe 6-1/4", With Hook and Spiral Probe | Integra® Miltex® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
8 | 10381780453093 | PM-4740 | PM-4740 | Spare Tubing For Worst Pigtail Probes (REF #'s PM-4739HK and PM-4739HL) | Integra® Miltex® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
9 | 10381780453086 | PM-4739HL | PM-4739HL | Worst Pigtail Probe 6-1/4", with Hole and Silicone Cannula | Integra® Miltex® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
10 | 10381780442790 | 40-92 | 40-92 | Probe and Packer 6", Blunt Probe and 2mm Packer | Integra® Miltex® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
11 | 10381780442776 | 40-89 | 40-89 | Probe and Excavator 6", Double-Ended, Blunt Probe and Blunt Hook End | Integra® Miltex® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
12 | 10381780280422 | 051002 | 051002 | MBA™ Titanium Subtalar Implant System PROBE | MBA™ Titanium Subtalar Implant System | ASCENSION ORTHOPEDICS, INC. |
13 | 10381780217718 | P4913 | P4913 | Bunnell Tendon Passer And Forwarding Probe, 9" | Integra® Jarit® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
14 | 10381780217701 | P4912 | P4912 | Bunnell Tendon Passer and Probe, 7-1/4" | Integra® Jarit® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
15 | 10381780193432 | P4740 | P4740 | Worst Pigtail Probe, Spare Tubing, Silicone For Ref# P4739HK and P4739HL | Integra® Jarit® | INTEGRA LIFESCIENCES PRODUCTION CORPORATION |
16 | M68120066000000 | 2006-66-0000 | 2006-66-0000 | Straight Pedicle Probe | Apelo® / Apelo® MIS | ATLAS SPINE, INC. |
17 | M68120065900000 | 2006-59-0000 | 2006-59-0000 | Curved Pedicle Probe | Apelo® / Apelo® MIS | ATLAS SPINE, INC. |
18 | M68120063100000 | 2006-31-0000 | 2006-31-0000 | Straight Sounding Probe | Apelo® / Apelo® MIS | ATLAS SPINE, INC. |
19 | M68120063000000 | 2006-30-0000 | 2006-30-0000 | Curved Sounding Probe | Apelo® / Apelo® MIS | ATLAS SPINE, INC. |
20 | 08806395401505 | GS110-0327 | GS110-0327 | Curved Thoracic Bone Probe | GSS™ and AnyPlus® | GS MEDICAL CO., LTD. |
21 | 08806395401499 | GS110-0326 | GS110-0326 | Curved Bone Probe Steffee Tip | GSS™ and AnyPlus® | GS MEDICAL CO., LTD. |
22 | 08806395401468 | GS110-0317 | GS110-0317 | Straight Thoracic Bone Probe | GSS™ and AnyPlus® | GS MEDICAL CO., LTD. |
23 | 08806395401451 | GS110-0316 | GS110-0316 | Straight Bone Probe Steffee Tip | GSS™ and AnyPlus® | GS MEDICAL CO., LTD. |
24 | M20922661 | 22661 | Horizon Subtalar Gen 2 Sizing Probe 12mm | BIOPRO, INC. | ||
25 | M20922660 | 22660 | Horizon Subtalar Gen 2 Sizing Probe 11mm | BIOPRO, INC. | ||
26 | M20922659 | 22659 | Horizon Subtalar Gen 2 Sizing Probe 10mm | BIOPRO, INC. | ||
27 | M20922658 | 22658 | Horizon Subtalar Gen 2 Sizing Probe 9mm | BIOPRO, INC. | ||
28 | M20922656 | 22656 | Horizon Subtalar Gen 2 Sizing Probe 7mm | BIOPRO, INC. | ||
29 | M20922655 | 22655 | Horizon Subtalar Gen 2 Sizing Probe 6mm | BIOPRO, INC. | ||
30 | M20922654 | 22654 | Horizon Subralar Gen 2 Removal Driver | BIOPRO, INC. | ||
31 | M20922653 | 22653 | Horizon Subtalar Gen 2 Hex Driver | BIOPRO, INC. | ||
32 | M20922652 | 22652 | Horixon Subtalar Gen 2 Instrument tray | BIOPRO, INC. | ||
33 | M20922650 | 22650 | Horizon Subtalar Gen 2 Starter Probe | BIOPRO, INC. | ||
34 | M20922567 | 22657 | Horizon Subtalar Gen 2 Sizing Probe 8mm | BIOPRO, INC. | ||
35 | M209174550 | 17455 | Starter Probe | BIOPRO, INC. | ||
36 | 08800037569714 | SF0450 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
37 | 08800037569707 | SF0460 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
38 | 08800037550903 | SFDS1003 | ANAX 5.5 Spinal System | U&I CORPORATION | ||
39 | 08800037546074 | OS0340 | ANAX™ OCT Spinal System | U&I CORPORATION | ||
40 | 08800037546067 | OS0330 | ANAX™ OCT Spinal System | U&I CORPORATION | ||
41 | 08800037544919 | SF0360 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
42 | 08800037544902 | SF0350 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
43 | 08800037542854 | SFD0100 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
44 | 08800037542847 | SFD0090 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
45 | 08800037542830 | SFD0080 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
46 | 08800037542823 | SFD0070 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
47 | 08800037527745 | SFS1058 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
48 | 08800037527738 | SFS1057 | ANAX™ 5.5 SPINAL SYSTEM | U&I CORPORATION | ||
49 | 08800037508157 | OS0340 | ANAX™ OCT SPINAL SYSTEM | U&I CORPORATION | ||
50 | 08800037508140 | OS0330 | ANAX™ OCT SPINAL SYSTEM | U&I CORPORATION |