Other products from "MEDICAL DESIGNS LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M364119902FD90 11-9902-FD9 18mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 18mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
2 M364119902FD80 11-9902-FD8 16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
3 M364119902FD70 11-9902-FD7 16mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 16mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
4 M364119902FD60 11-9902-FD6 14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
5 M364119902FD50 11-9902-FD5 14mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 14mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
6 M364119902FD40 11-9902-FD4 12mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 12mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
7 M364119902FD30 11-9902-FD3 12mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 12mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
8 M364119902FD20 11-9902-FD2 10mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 10mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
9 M364119902FD100 11-9902-FD10 18mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 18mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Asfora Bullet Cage® System
10 M364119902FD10 11-9902-FD1 10mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedu 10mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation. MAX Intervertebral Fusion Device With Bone Graft, Lumbar Asfora Bullet Cage® System
11 M364111109FD920 11-1109-FD9-2 Adjustable Drill Collar OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
12 M364111109FD910 11-1109-FD9-1 Drill Bit OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
13 M364111109FD820 11-1109-FD8-2 Packing Tube OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
14 M364111109FD810 11-1109-FD8-1 Packing Plunger OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
15 M364111109FD730 11-1109-FD7-3 Parallel Guide Sliding Block OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
16 M364111109FD720 11-1109-FD7-2 Parallel Guide Locking Nut OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
17 M364111109FD710 11-1109-FD7-1 Parallel Guide Frame OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
18 M364111109FD211 11-1109-FD21 Long Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
19 M364111109FD201 11-1109-FD20 Short Blunt Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
20 M364111109FD190 11-1109-FD19 Sterilization Case OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
21 M364111109FD180 11-1109-FD18 Drill Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
22 M364111109FD170 11-1109-FD17 Torx Bit T-Handle OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
23 M364111109FD161 11-1109-FD16 Sharp Steinmann Pin OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone SAMBA SCREW SYSTEM
24 M364111109FD150 11-1109-FD15 Plunger Distance Tool OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
25 M364111109FD140 11-1109-FD14 Cannulated Torx Driver Bit OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
26 M364111109FD130 11-1109-FD13 Striker Tube OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
27 M364111109FD110 11-1109-FD11 Pin Sleeve OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
28 M364111109FD100 11-1109-FD10 Drill Guide OUR,HWC Sacroiliac Joint Fixation,Screw, Fixation, Bone 2 SAMBA SCREW SYSTEM
29 M111109FD120 11-1109-FD12 Drill Gauge HWC,OUR Screw, Fixation, Bone,Sacroiliac Joint Fixation 2 SAMBA SCREW SYSTEM
30 M364111106FD9160 11-1106-FD9-16 16mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
31 M364111106FD9140 11-1106-FD9-14 14mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
32 M364111106FD9120 11-1106-FD9-12 12mm Variable Angle Rescue Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
33 M364111106FD8160 11-1106-FD8-16 16mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
34 M364111106FD8140 11-1106-FD8-14 14mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
35 M364111106FD8120 11-1106-FD8-12 12mm Fixed Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
36 M364111106FD7160 11-1106-FD7-16 16mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
37 M364111106FD7140 11-1106-FD7-14 14mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
38 M364111106FD7120 11-1106-FD7-12 12mm Variable Angle Locking Screw KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
39 M364111106FD4940 11-1106-FD4-94 4 Level, 94mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 94mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
40 M364111106FD4900 11-1106-FD4-90 4 Level, 90mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 90mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
41 M364111106FD4860 11-1106-FD4-86 4 Level, 86mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 86mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
42 M364111106FD4820 11-1106-FD4-82 4 Level, 82mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 82mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
43 M364111106FD4780 11-1106-FD4-78 4 Level, 78mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 78mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
44 M364111106FD4740 11-1106-FD4-74 4 Level, 74mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 4 Level, 74mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
45 M364111106FD430 11-1106-FD43 Axial Driver Handle KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
46 M364111106FD420 11-1106-FD42 Axial Drill Bit Handle KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
47 M364111106FD410 11-1106-FD41 Fixed Angle Drill Guide KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
48 M364111106FD3750 11-1106-FD3-75 3 Level, 75mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 75mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
49 M364111106FD3720 11-1106-FD3-72 3 Level, 72mm Cervical Plate; The Asfora Anterior Cervical Plate System is inten 3 Level, 72mm Cervical Plate; The Asfora Anterior Cervical Plate System is intended to provide temporarystabilization to the anterior spine during the development of cervical spinefusions (C2-T1) for the following indications: degenerative disc disease (DDD)(defined as neck pain of discogenic origin with degeneration of the discconfirmed by history and radiographic studies), spondylolisthesis, trauma (i.e.,fracture or dislocation), spinal stenosis, deformities or curvatures (i.e., scoliosis,kyphosis, and/or lordosis), tumor, pseudoarthrosis, and failed previous fusion. KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
50 M364111106FD370 11-1106-FD37 Sterilization Case KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Asfora Anterior Cervical Plate System
Other products with the same Product Codes "OUR, HWC"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 04050659536531 SO-1002-17 TI Snap-off Screw,self-drilling+ _x000D_tapping,17mm TI Snap-off Screw,self-drilling+ _x000D_tapping,17mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
2 04050659536517 SO-1002-16 TI Snap-off Screw,self-drilling+ _x000D_tapping,16mm TI Snap-off Screw,self-drilling+ _x000D_tapping,16mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
3 04050659536494 SO-1002-15 TI Snap-off Screw,self-drilling+ _x000D_tapping,15mm TI Snap-off Screw,self-drilling+ _x000D_tapping,15mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
4 04050659536470 SO-1002-14 TI Snap-off Screw,self-drilling+ _x000D_tapping,14mm TI Snap-off Screw,self-drilling+ _x000D_tapping,14mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
5 04050659536456 SO-1002-13 TI Snap-off Screw,self-drilling+ _x000D_tapping,13mm TI Snap-off Screw,self-drilling+ _x000D_tapping,13mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
6 04050659536432 SO-1002-12 TI Snap-off Screw,self-drilling+ _x000D_tapping,12mm TI Snap-off Screw,self-drilling+ _x000D_tapping,12mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
7 04050659536418 SO-1002-11 TI Snap-off Screw,self-drilling+ _x000D_tapping,11mm TI Snap-off Screw,self-drilling+ _x000D_tapping,11mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
8 04050659536395 SO-1002-10 TI Snap-off Screw,self-drilling+ _x000D_tapping,10mm TI Snap-off Screw,self-drilling+ _x000D_tapping,10mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
9 04050659485921 KW-1000-080 HBS-Guide Wire ø 1.0x80mm _x000D_ HBS-Guide Wire ø 1.0x80mm _x000D_ _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
10 04050659465794 HBS-1003-30S TI HBS self-drilling high compression _x000D_screw,cannulated,30mm TI HBS self-drilling high compression _x000D_screw,cannulated,30mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
11 04050659465770 HBS-1003-28S TI HBS self-drilling high compression _x000D_screw,cannulated,28mm TI HBS self-drilling high compression _x000D_screw,cannulated,28mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
12 04050659465756 HBS-1003-26S TI HBS self-drilling high compression _x000D_screw,cannulated,26mm TI HBS self-drilling high compression _x000D_screw,cannulated,26mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
13 04050659465732 HBS-1003-24S TI HBS self-drilling high compression _x000D_screw,cannulated,24mm TI HBS self-drilling high compression _x000D_screw,cannulated,24mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
14 04050659465718 HBS-1003-22S TI HBS self-drilling high compression _x000D_screw,cannulated,22mm TI HBS self-drilling high compression _x000D_screw,cannulated,22mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
15 04050659465695 HBS-1003-20S TI HBS self-drilling high compression _x000D_screw,cannulated,20mm TI HBS self-drilling high compression _x000D_screw,cannulated,20mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
16 04050659465671 HBS-1003-18S TI HBS self-drilling high compression _x000D_screw,cannulated,18mm TI HBS self-drilling high compression _x000D_screw,cannulated,18mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
17 04050659465657 HBS-1003-16S TI HBS self-drilling high compression _x000D_screw,cannulated,16mm TI HBS self-drilling high compression _x000D_screw,cannulated,16mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
18 04050659465633 HBS-1003-14S TI HBS self-drilling high compression _x000D_screw,cannulated,14mm TI HBS self-drilling high compression _x000D_screw,cannulated,14mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
19 04050659465619 HBS-1003-12S TI HBS self-drilling high compression _x000D_screw,cannulated,12mm TI HBS self-drilling high compression _x000D_screw,cannulated,12mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
20 04050659465596 HBS-1003-10S TI HBS self-drilling high compression _x000D_screw,cannulated,10mm TI HBS self-drilling high compression _x000D_screw,cannulated,10mm _x000D_Ø3.2/2.5mm mahe medical GmbH MAHE MEDICAL GMBH
21 04050659465510 HBS-1002-40S TI HBS self-drilling high compression _x000D_screw,cannulated,40mm TI HBS self-drilling high compression _x000D_screw,cannulated,40mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
22 04050659465497 HBS-1002-38S TI HBS self-drilling high compression _x000D_screw,cannulated,38mm TI HBS self-drilling high compression _x000D_screw,cannulated,38mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
23 04050659465473 HBS-1002-36S TI HBS self-drilling high compression _x000D_screw,cannulated,36mm TI HBS self-drilling high compression _x000D_screw,cannulated,36mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
24 04050659465459 HBS-1002-34S TI HBS self-drilling high compression _x000D_screw,cannulated,34mm TI HBS self-drilling high compression _x000D_screw,cannulated,34mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
25 04050659465435 HBS-1002-32S TI HBS self-drilling high compression _x000D_screw,cannulated,32mm TI HBS self-drilling high compression _x000D_screw,cannulated,32mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
26 04050659465411 HBS-1002-30S TI HBS self-drilling high compression _x000D_screw,cannulated,30mm TI HBS self-drilling high compression _x000D_screw,cannulated,30mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
27 04050659465398 HBS-1002-28S TI HBS self-drilling high compression _x000D_screw,cannulated,28mm TI HBS self-drilling high compression _x000D_screw,cannulated,28mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
28 04050659465374 HBS-1002-26S TI HBS self-drilling high compression _x000D_screw,cannulated,26mm TI HBS self-drilling high compression _x000D_screw,cannulated,26mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
29 04050659465350 HBS-1002-24S TI HBS self-drilling high compression _x000D_screw,cannulated,24mm TI HBS self-drilling high compression _x000D_screw,cannulated,24mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
30 04050659465336 HBS-1002-22S TI HBS self-drilling high compression _x000D_screw,cannulated,22mm TI HBS self-drilling high compression _x000D_screw,cannulated,22mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
31 04050659465329 HBS-1002-20S-ST5 TI HBS self-drilling high compression _x000D_screw,cannulated,20mm,5 pcs./unit TI HBS self-drilling high compression _x000D_screw,cannulated,20mm,5 pcs./unit _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
32 04050659465305 HBS-1002-20S TI HBS self-drilling high compression _x000D_screw,cannulated,20mm TI HBS self-drilling high compression _x000D_screw,cannulated,20mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
33 04050659465282 HBS-1002-18S-ST5 TI HBS self-drilling high compression _x000D_screw,cannulated,18mm,5 pcs./unit TI HBS self-drilling high compression _x000D_screw,cannulated,18mm,5 pcs./unit _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
34 04050659465268 HBS-1002-18S TI HBS self-drilling high compression _x000D_screw,cannulated,18mm TI HBS self-drilling high compression _x000D_screw,cannulated,18mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
35 04050659465251 HBS-1002-16S-ST5 TI HBS self-drilling high compression _x000D_screw,cannulated,16mm,5 pcs./unit TI HBS self-drilling high compression _x000D_screw,cannulated,16mm,5 pcs./unit _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
36 04050659465237 HBS-1002-16S TI HBS self-drilling high compression _x000D_screw,cannulated,16mm TI HBS self-drilling high compression _x000D_screw,cannulated,16mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
37 04050659465213 HBS-1002-14S TI HBS self-drilling high compression _x000D_screw,cannulated,14mm TI HBS self-drilling high compression _x000D_screw,cannulated,14mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
38 04050659465190 HBS-1002-12S TI HBS self-drilling high compression _x000D_screw,cannulated,12mm TI HBS self-drilling high compression _x000D_screw,cannulated,12mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
39 04050659433731 932999016 Dia. 7.0/3.9mm Washer s/s _x000D_ Dia. 7.0/3.9mm Washer s/s _x000D_ _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
40 04050659433724 932999015 6.5mm Washer s/s for 2.7mm screws _x000D_ 6.5mm Washer s/s for 2.7mm screws _x000D_ _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
41 04050659433717 932999014 2.7mm Ligament Washer-Spiked _x000D_ 2.7mm Ligament Washer-Spiked _x000D_ _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
42 04050659433250 931140014 Cancellous screws (full thread),4.0/14mm_x000D_'fat neck' Cancellous screws (full thread),4.0/14mm_x000D_'fat neck' _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
43 04050659432741 930545034 Screw 4.5 x 34mm s/s _x000D_self-tapping Screw 4.5 x 34mm s/s _x000D_self-tapping _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
44 04050659432710 930545028 Screw 4.5 x 28mm s/s _x000D_self-tapping Screw 4.5 x 28mm s/s _x000D_self-tapping _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
45 04050659432680 930545022 Screw 4.5 x 22mm s/s _x000D_self-tapping Screw 4.5 x 22mm s/s _x000D_self-tapping _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
46 04050659337039 150-6635-056PTXL TI 3.5mm mono-/polyaxial locking screw, _x000D_L.56mm TI 3.5mm mono-/polyaxial locking screw, _x000D_L.56mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
47 04050659337008 150-6635-050PTXL TI 3.5mm mono-/polyaxial locking screw, _x000D_L.50mm TI 3.5mm mono-/polyaxial locking screw, _x000D_L.50mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
48 04050659336995 150-6635-048PTXL TI 3.5mm mono-/polyaxial locking screw, _x000D_L.48mm TI 3.5mm mono-/polyaxial locking screw, _x000D_L.48mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
49 04050659336988 150-6635-046PTXL TI 3.5mm mono-/polyaxial locking screw, _x000D_L.46mm TI 3.5mm mono-/polyaxial locking screw, _x000D_L.46mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH
50 04050659336971 150-6635-044PTXL TI 3.5mm mono-/polyaxial locking screw, _x000D_L.44mm TI 3.5mm mono-/polyaxial locking screw, _x000D_L.44mm _x000D_ mahe medical GmbH MAHE MEDICAL GMBH