Other products from "U&I CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 08800015947732 SS0220 FZX Guide, surgical, instrument 1 Perfix™ MIS
2 08800037551696 TSA6407S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
3 08800037551689 TSA6406S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
4 08800037551672 TSA6405S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
5 08800037551665 TSA6211S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
6 08800037551658 TSA6210S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
7 08800037551641 TSA6209S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
8 08800037551634 TSA6208S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
9 08800037551627 TSA6207S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
10 08800037551610 TSA6206S OVE Intervertebral fusion device with integrated fixation, cervical 2 Velofix™ SA Cervical Cage
11 08800037551603 35012 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
12 08800037551597 35011 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
13 08800037551580 35010 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
14 08800037551573 35009 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
15 08800037551566 35008 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
16 08800037551559 35007 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
17 08800037551542 35006 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
18 08800037551535 35005 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
19 08800037551528 35004 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
20 08800037551511 35003 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
21 08800037551504 35002 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
22 08800037551498 35001 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
23 08800037551481 32074 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
24 08800037551474 32143 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
25 08800037551467 32073 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
26 08800037551450 32142 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
27 08800037551443 32072 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
28 08800037551436 32141 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
29 08800037551429 32071 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
30 08800037551412 32140 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
31 08800037551405 32070 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
32 08800037551399 32139 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
33 08800037551382 32069 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
34 08800037551375 32138 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
35 08800037551368 32068 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
36 08800037551351 32137 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
37 08800037551344 32067 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
38 08800037551337 32136 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
39 08800037551320 32066 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
40 08800037551313 32135 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
41 08800037551306 32065 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
42 08800037551290 32134 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
43 08800037551283 32064 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
44 08800037551276 32133 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
45 08800037551269 32063 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
46 08800037551252 32132 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
47 08800037551245 32062 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
48 08800037551238 32131 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
49 08800037551221 32061 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
50 08800037551214 32130 HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Dyna Locking Trochanteric Nail™
Other products with the same Product Code "MAX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 08806378300900 1101-1012 1101-1012 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
2 08806378300894 1101-1011 1101-1011 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
3 08806378300887 1101-1010 1101-1010 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
4 08806378300870 1101-1009 1101-1009 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
5 08806378300863 1101-1008 1101-1008 "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available i "The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560). The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine." AnyPlus PEEK Lumbar Fusion Cage GS MEDICAL CO., LTD.
6 08806373874192 SI.C10.0010 ACIF HOLDER STOPPER TYPE LOSPA IS Spinal System CORENTEC CO., LTD
7 08806373871825 SI.C50.6816 T-PLIF TRIAL 8° 34 X 10 X 16 LOSPA IS Spinal System CORENTEC CO., LTD
8 08806373871818 SI.C50.6815 T-PLIF TRIAL 8° 34 X 10 X 15 LOSPA IS Spinal System CORENTEC CO., LTD
9 08806373871801 SI.C50.6814 T-PLIF TRIAL 8° 34 X 10 X 14 LOSPA IS Spinal System CORENTEC CO., LTD
10 08806373871795 SI.C50.6813 T-PLIF TRIAL 8° 34 X 10 X 13 LOSPA IS Spinal System CORENTEC CO., LTD
11 08806373871788 SI.C50.6812 T-PLIF TRIAL 8° 34 X 10 X 12 LOSPA IS Spinal System CORENTEC CO., LTD
12 08806373871771 SI.C50.6416 T-PLIF TRIAL 4° 34 X 10 X 16 LOSPA IS Spinal System CORENTEC CO., LTD
13 08806373871764 SI.C50.6415 T-PLIF TRIAL 4° 34 X 10 X 15 LOSPA IS Spinal System CORENTEC CO., LTD
14 08806373871757 SI.C50.6414 T-PLIF TRIAL 4° 34 X 10 X 14 LOSPA IS Spinal System CORENTEC CO., LTD
15 08806373871740 SI.C50.6413 T-PLIF TRIAL 4° 34 X 10 X 13 LOSPA IS Spinal System CORENTEC CO., LTD
16 08806373871733 SI.C50.6412 T-PLIF TRIAL 4° 34 X 10 X 12 LOSPA IS Spinal System CORENTEC CO., LTD
17 08806373871726 SI.C50.6411 T-PLIF TRIAL 4° 34 X 10 X 11 LOSPA IS Spinal System CORENTEC CO., LTD
18 08806373871719 SI.C50.6410 T-PLIF TRIAL 4° 34 X 10 X 10 LOSPA IS Spinal System CORENTEC CO., LTD
19 08806373871702 SI.C50.6409 T-PLIF TRIAL 4° 34 X 10 X 09 LOSPA IS Spinal System CORENTEC CO., LTD
20 08806373871696 SI.C50.6016 T-PLIF TRIAL 0° 34 X 10 X 16 LOSPA IS Spinal System CORENTEC CO., LTD
21 08806373871689 SI.C50.6015 T-PLIF TRIAL 0° 34 X 10 X 15 LOSPA IS Spinal System CORENTEC CO., LTD
22 08806373871672 SI.C50.6014 T-PLIF TRIAL 0° 34 X 10 X 14 LOSPA IS Spinal System CORENTEC CO., LTD
23 08806373871665 SI.C50.6013 T-PLIF TRIAL 0° 34 X 10 X 13 LOSPA IS Spinal System CORENTEC CO., LTD
24 08806373871658 SI.C50.6012 T-PLIF TRIAL 0° 34 X 10 X 12 LOSPA IS Spinal System CORENTEC CO., LTD
25 08806373871641 SI.C50.6011 T-PLIF TRIAL 0° 34 X 10 X 11 LOSPA IS Spinal System CORENTEC CO., LTD
26 08806373871634 SI.C50.6010 T-PLIF TRIAL 0° 34 X 10 X 10 LOSPA IS Spinal System CORENTEC CO., LTD
27 08806373871627 SI.C50.6009 T-PLIF TRIAL 0° 34 X 10 X 09 LOSPA IS Spinal System CORENTEC CO., LTD
28 08806373871610 SI.C50.6008 T-PLIF TRIAL 0° 34 X 10 X 08 LOSPA IS Spinal System CORENTEC CO., LTD
29 08806373871603 SI.C50.5816 T-PLIF TRIAL 8° 31 X 10 X 16 LOSPA IS Spinal System CORENTEC CO., LTD
30 08806373871597 SI.C50.5815 T-PLIF TRIAL 8° 31 X 10 X 15 LOSPA IS Spinal System CORENTEC CO., LTD
31 08806373871580 SI.C50.5814 T-PLIF TRIAL 8° 31 X 10 X 14 LOSPA IS Spinal System CORENTEC CO., LTD
32 08806373871573 SI.C50.5813 T-PLIF TRIAL 8° 31 X 10 X 13 LOSPA IS Spinal System CORENTEC CO., LTD
33 08806373871566 SI.C50.5812 T-PLIF TRIAL 8° 31 X 10 X 12 LOSPA IS Spinal System CORENTEC CO., LTD
34 08806373871559 SI.C50.5811 T-PLIF TRIAL 8° 31 X 10 X 11 LOSPA IS Spinal System CORENTEC CO., LTD
35 08806373871542 SI.C50.5810 T-PLIF TRIAL 8° 31 X 10 X 10 LOSPA IS Spinal System CORENTEC CO., LTD
36 08806373871535 SI.C50.5416 T-PLIF TRIAL 4° 31 X 10 X 16 LOSPA IS Spinal System CORENTEC CO., LTD
37 08806373871528 SI.C50.5415 T-PLIF TRIAL 4° 31 X 10 X 15 LOSPA IS Spinal System CORENTEC CO., LTD
38 08806373871511 SI.C50.5414 T-PLIF TRIAL 4° 31 X 10 X 14 LOSPA IS Spinal System CORENTEC CO., LTD
39 08806373871504 SI.C50.5413 T-PLIF TRIAL 4° 31 X 10 X 13 LOSPA IS Spinal System CORENTEC CO., LTD
40 08806373871498 SI.C50.5412 T-PLIF TRIAL 4° 31 X 10 X 12 LOSPA IS Spinal System CORENTEC CO., LTD
41 08806373871481 SI.C50.5411 T-PLIF TRIAL 4° 31 X 10 X 11 LOSPA IS Spinal System CORENTEC CO., LTD
42 08806373871474 SI.C50.5410 T-PLIF TRIAL 4° 31 X 10 X 10 LOSPA IS Spinal System CORENTEC CO., LTD
43 08806373871467 SI.C50.5409 T-PLIF TRIAL 4° 31 X 10 X 09 LOSPA IS Spinal System CORENTEC CO., LTD
44 08806373871450 SI.C50.5016 T-PLIF TRIAL 0° 31 X 10 X 16 LOSPA IS Spinal System CORENTEC CO., LTD
45 08806373871443 SI.C50.5015 T-PLIF TRIAL 0° 31 X 10 X 15 LOSPA IS Spinal System CORENTEC CO., LTD
46 08806373871436 SI.C50.5014 T-PLIF TRIAL 0° 31 X 10 X 14 LOSPA IS Spinal System CORENTEC CO., LTD
47 08806373871429 SI.C50.5013 T-PLIF TRIAL 0° 31 X 10 X 13 LOSPA IS Spinal System CORENTEC CO., LTD
48 08806373871412 SI.C50.5012 T-PLIF TRIAL 0° 31 X 10 X 12 LOSPA IS Spinal System CORENTEC CO., LTD
49 08806373871405 SI.C50.5011 T-PLIF TRIAL 0° 31 X 10 X 11 LOSPA IS Spinal System CORENTEC CO., LTD
50 08806373871399 SI.C50.5010 T-PLIF TRIAL 0° 31 X 10 X 10 LOSPA IS Spinal System CORENTEC CO., LTD