SEARCH RESULTS FOR: Origin(1500 results)
REGL - Regular Non-Extendable Smoke Evacuation Pencil, Non-stick Ceramic Coated Blade, Holster, 10' Hose (1pc)
Medisourcenet, Inc
REGL
In Commercial Distribution
- 10850034735044 ()
- 00850034735047 ()
- Open-surgery electrosurgical handpiece/electrode, monopolar, reusable
- Surgical plume evacuation system
microTargeting Frame Kit D.ZAP/Lead Insertion, 1x, Sterile, for use with mT Drive or STar Drive.
Contains:
34685L: Single D.ZAP Electrode.
66-DA-SD: Drape Sleeve.
66-EL-LP: Patient Lead for LP+.
66-IT-05P: Single Insertion Tube Set.
FHC, INC.
KT-FPK-S20-00508
In Commercial Distribution
- 00873263005088 ()
KT-FPK-S20
- Depth electrode
- Neurological stereotactic surgery system
- Intracerebral cannula, implantable
microTargeting Single Procedure Kit, with microElectrode, tubes, sterile drape sleeve and cable.
Contains:
IT(BP2): Insertion Tube.
2x MTDWLN(BP)(BP7): microTargeting Electrode.
PT(BP2): Protective Tube.
Sterile Drape Sleeve for microTargeting motor
FC1020 Electrode Lead
Individual Specifications:
IT(BP2) - 183mm tube length, 1.829mm OD, 1.6mm ID, 184mm stylet (not including collar).
MTDWLN(BP)(BP7) - 271.4mm electrode length, 10mm differential, 256.4mm protective tube length, 0.77mm OD. 1Meg DZAP(L)
PT(PB2) - 181mm tube length, 1.47mm OD, 0.99mm ID
OD: 0.77mm
FHC, INC.
KTF1001-00133
Not in Commercial Distribution
- 00873263001332 ()
KTF1001
- Patient surgical drape, single-use
- Intracerebral cannula, implantable
- Depth electrode
microTargeting Platform Procedure Consumables Kit, 1x, sterile, for use with mT or STar Drive, mT Platform and Guideline 4000 LP+.
Contains:
44975L: D.ZAP Tungsten Differential Electrode - - 220.72mm electrode length, 10mm differential, 205.72mm protective tube length, DZAP(L) 1Meg, 0.55mm od.
66-DA-SD: Sterile Drape Sleeve for motor
66-EL-LP: Patient Lead for Guideline 4000 LP+
66-IT-03P: Sterile Single Insertion Tube Set -
IT(MP1) - 184.1mm tube length, 1.83mm od, 1.6mm id with Stylet
PT(MP1) - Diameter reduction tube 0.58mm id
FHC, INC.
KT-PPK-S-00366
In Commercial Distribution
- 00873263003664 ()
KT-PPK-S
- Depth electrode
- Patient surgical drape, single-use
- Intracerebral cannula, implantable
microTargeting Single Procedure Kit, with microElectrode, tubes, sterile drape sleeve and cable.
Contains:
IT(BP2): Insertion Tube.
2x MTDWLN(BP)(BP7): microTargeting Electrode.
PT(BP2): Protective Tube.
Sterile Drape Sleeve for microTargeting motor
FC1020 Electrode Lead
Individual Specifications:
IT(BP2) - 183mm tube length, 1.829mm OD, 1.6mm ID, 184mm stylet (not including collar).
MTDWLN(BP)(BP7) - 271.4mm electrode length, 10mm differential, 256.4mm protective tube length, 0.77mm OD. 1Meg DZAP(L)
PT(PB2) - 181mm tube length, 1.47mm OD, 0.99mm ID
OD: 0.77mm
FHC, INC.
KTF1001-00757
In Commercial Distribution
- 00873263007570 ()
KTF1001
- Depth electrode
- Patient surgical drape, single-use
- Intracerebral cannula, nonimplantable, single-use
primaLOK SP 18mm Implant Assembly, Sterile
The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use.
Wenzel Spine, Inc.
800-0118-00
In Commercial Distribution
- 00813210021778 ()
- Height: 18 Millimeter
- Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial
primaLOK SP 12mm Implant Assembly, Sterile
The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as ack pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use.
Wenzel Spine, Inc.
800-0112-00
In Commercial Distribution
- 00813210021754 ()
- Height: 12 Millimeter
- Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial
primaLOK SP 15mm Implant Assembly, Sterile
The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as ack pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use.
Wenzel Spine, Inc.
800-0115-00
In Commercial Distribution
- 00813210021761 ()
- Height: 15 Millimeter
- Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial
primaLOK SP 10mm Implant Assembly, Sterile
The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as ack pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use.
Wenzel Spine, Inc.
800-0110-00
In Commercial Distribution
- 00813210021747 ()
- Height: 10 Millimeter
- Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial
primaLOK SP 8mm Implant Assembly, Sterile
The Wenzel Spine primaLOK SP Interspinous Fusion System is a posterior, nonpedicle supplemental fixation device, intended for use in the non-cervical spine (T1-S1). it is intended for plate fixation/attachment to spinous process for the purpose of achieving supplemental fusion in the following conditions: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e. fracture or dislocation), and/or tumor. The primaLOK SP Interspinous Fusion System is intended for use at one level with bone graft material and not intended for stand-alone use.
Wenzel Spine, Inc.
800-0108-00
In Commercial Distribution
- 00813210021730 ()
- Height: 8 Millimeter
- Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial