SEARCH RESULTS FOR: Origin(1499 results)
No Description
Ad-Tech Medical Instrument Corporation
CNE1-2KDINX
In Commercial Distribution
- 90841823100859 ()
- 00841823100856 ()
CNE1-2KDINX
- Depth electrode
No Description
Ad-Tech Medical Instrument Corporation
CNE1-3KDINX
In Commercial Distribution
- 90841823100866 ()
- 00841823100863 ()
CNE1-3KDINX
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 8 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-08-121
In Commercial Distribution
- 00650551041481 ()
- Recording Depth: 72 Millimeter
- Outer Diameter: 1.8 Millimeter
- Spacing: 10 Millimeter
2101-08-121
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 8 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-08-120
In Commercial Distribution
- 00650551041474 ()
- Recording Depth: 37 Millimeter
- Outer Diameter: 1.8 Millimeter
- Spacing: 5 Millimeter
2101-08-120
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 6 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-06-121
In Commercial Distribution
- 00650551041306 ()
- Outer Diameter: 1.8 Millimeter
- Spacing: 10 Millimeter
- Recording Depth: 52 Millimeter
2101-06-121
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 4 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-04-121
In Commercial Distribution
- 00650551041108 ()
- Outer Diameter: 1.8 Millimeter
- Spacing: 10 Millimeter
- Recording Depth: 32 Millimeter
2101-04-121
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 2 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-02-121
In Commercial Distribution
- 00650551040927 ()
- Outer Diameter: 1.8 Millimeter
- Spacing: 10 Millimeter
- Recording Depth: 12 Millimeter
2101-02-121
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 2 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-02-120
In Commercial Distribution
- 00650551040910 ()
- Spacing: 5 Millimeter
- Recording Depth: 7 Millimeter
- Outer Diameter: 1.8 Millimeter
2101-02-120
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 8 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-08-120
In Commercial Distribution
- 00650551040699 ()
- Spacing: 5 Millimeter
- Recording Depth: 37 Millimeter
- Outer Diameter: 1.8 Millimeter
2102-08-120
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 6 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-06-120
In Commercial Distribution
- 00650551040507 ()
- Outer Diameter: 1.8 Millimeter
- Spacing: 5 Millimeter
- Recording Depth: 27 Millimeter
2102-06-120
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 2 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-02-121
In Commercial Distribution
- 00650551040118 ()
- Spacing: 10 Millimeter
- Outer Diameter: 1.8 Millimeter
- Recording Depth: 12 Millimeter
2102-02-121
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 2 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-02-120
In Commercial Distribution
- 00650551040101 ()
- Recording Depth: 7 Millimeter
- Outer Diameter: 1.8 Millimeter
- Spacing: 5 Millimeter
2102-02-120
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 6 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-06-120
In Commercial Distribution
- 00650551041290 ()
- Spacing: 5 Millimeter
- Recording Depth: 27 Millimeter
- Outer Diameter: 1.8 Millimeter
2101-06-120
- Depth electrode
DEPTH ELECTRODE, STAINLESS STEEL, 4 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2101-04-120
In Commercial Distribution
- 00650551041092 ()
- Spacing: 5 Millimeter
- Recording Depth: 17 Millimeter
- Outer Diameter: 1.8 Millimeter
2101-04-120
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 8 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-08-121
In Commercial Distribution
- 00650551040705 ()
- Outer Diameter: 1.8 Millimeter
- Spacing: 10 Millimeter
- Recording Depth: 72 Millimeter
2102-08-121
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 6 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-06-121
In Commercial Distribution
- 00650551040514 ()
- Recording Depth: 52 Millimeter
- Outer Diameter: 1.8 Millimeter
- Spacing: 10 Millimeter
2102-06-121
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 4 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-04-121
In Commercial Distribution
- 00650551040309 ()
- Spacing: 10 Millimeter
- Recording Depth: 32 Millimeter
- Outer Diameter: 1.8 Millimeter
2102-04-121
- Depth electrode
DEPTH ELECTRODE, PLATINUM, 4 CONTACT (2MM), INLINE CONNECTOR
PMT CORPORATION
2102-04-120
In Commercial Distribution
- 00650551040293 ()
- Outer Diameter: 1.8 Millimeter
- Spacing: 5 Millimeter
- Recording Depth: 17 Millimeter
2102-04-120
- Depth electrode
Smoke Attachment Extender
Covidien LP
E3595
In Commercial Distribution
- 10884524001814 ()
- 20884524001811 ()
- Surgical plume evacuation system
Smoke Attachment
Covidien LP
E3590
In Commercial Distribution
- 20884524000296 ()
- 10884524000299 ()
- Surgical plume evacuation system
AlboSure Vascular Patch 2x9 cm
Lemaitre Vascular, Inc.
AP20090R
In Commercial Distribution
- 00840663105021 ()
AP20090R
- Cardiovascular patch, animal-derived
AlboSure Vascular Patch 1x 15 cm
Lemaitre Vascular, Inc.
AP10150R
In Commercial Distribution
- 00840663104895 ()
AP10150R
- Cardiovascular patch, animal-derived
AlboSure Vascular Patch 1x 10 cm
Lemaitre Vascular, Inc.
AP10100R
In Commercial Distribution
- 00840663104802 ()
AP10100R
- Cardiovascular patch, animal-derived
AlboSure Vascular Patch 1x 7.5 cm
Lemaitre Vascular, Inc.
AP10075T
In Commercial Distribution
- 00840663104765 ()
AP10075T
- Cardiovascular patch, animal-derived
AlboSure Vascular Patch 0.8x 7.5 cm
Lemaitre Vascular, Inc.
AP08075T
In Commercial Distribution
- 00840663104604 ()
AP08075T
- Cardiovascular patch, animal-derived
AlboSure Vascular Patch 0.6x 7.5 cm
Lemaitre Vascular, Inc.
AP06075T
In Commercial Distribution
- 00840663104543 ()
AP06075T
- Cardiovascular patch, animal-derived
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.
MEDICAL DESIGNS LLC
11-9902-FD9
In Commercial Distribution
- 1199029 ()
- M364119902FD90 ()
- Outer Diameter: 18 Millimeter
- Length: 21 Millimeter
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD8
In Commercial Distribution
- 1199028 ()
- M364119902FD80 ()
- Outer Diameter: 16 Millimeter
- Length: 25 Millimeter
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD7
In Commercial Distribution
- M364119902FD70 ()
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD6
In Commercial Distribution
- 1199026 ()
- M364119902FD60 ()
- Outer Diameter: 14 Millimeter
- Length: 25 Millimeter
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD5
In Commercial Distribution
- 1199025 ()
- M364119902FD50 ()
- Outer Diameter: 14 Millimeter
- Length: 21 Millimeter
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD4
In Commercial Distribution
- 1199024 ()
- M364119902FD40 ()
- Outer Diameter: 12 Millimeter
- Length: 25 Millimeter
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD3
In Commercial Distribution
- 1199023 ()
- M364119902FD30 ()
- Outer Diameter: 12 Millimeter
- Length: 21 Millimeter
- Metallic spinal interbody fusion cage
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
MEDICAL DESIGNS LLC
11-9902-FD2
In Commercial Distribution
- 1199022 ()
- M364119902FD20 ()
- Outer Diameter: 10 Millimeter
- Length: 25 Millimeter
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD10
In Commercial Distribution
- 11990210 ()
- M364119902FD100 ()
- Outer Diameter: 18 Millimeter
- Length: 25 Millimeter
- Metallic spinal interbody fusion cage
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.
MEDICAL DESIGNS LLC
11-9902-FD1
In Commercial Distribution
- M364119902FD10 ()
- 1199021 ()
- Length: 21 Millimeter
- Outer Diameter: 10 Millimeter
- Metallic spinal interbody fusion cage
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU8D5L25
Not in Commercial Distribution
- M272AU8D5L251 ()
- 10381780036531 ()
- 8 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU8D10L5
Not in Commercial Distribution
- M272AU8D10L51 ()
- 10381780036524 ()
- 8 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU8D10L25
Not in Commercial Distribution
- M272AU8D10L251 ()
- 10381780036517 ()
- 8 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU6D5L25
Not in Commercial Distribution
- M272AU6D5L251 ()
- 10381780036456 ()
- 6 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU6D10L5
Not in Commercial Distribution
- M272AU6D10L51 ()
- 10381780036449 ()
- 6 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU6D10L25
Not in Commercial Distribution
- M272AU6D10L251 ()
- 10381780036432 ()
- 6 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU12D5L25
Not in Commercial Distribution
- M272AU12D5L251 ()
- 10381780036111 ()
- 12 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU10D5L25
Not in Commercial Distribution
- M272AU10D5L251 ()
- 10381780036104 ()
- 10 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU4D5L25
Not in Commercial Distribution
- M272AU4D5L251 ()
- 10381780036326 ()
- 4 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU4D10L5
Not in Commercial Distribution
- M272AU4D10L51 ()
- 10381780036319 ()
- 4 platinum contacts
- Depth electrode
The Auragen™ depth electrodes are designed for intraoperative monitoring of cortical electrical activity in order to define the location of epileptogenic foci. They are inserted stereotaxically into the brain. Depth electrodes are available with 4 to 12 platinum/iridium contacts. The type of depth electrode used is dependent on the procedure and the size of area being tested.
INTEGRA NEUROSCIENCES IMPLANT (FRANCE)
AU4D10L25
Not in Commercial Distribution
- M272AU4D10L251 ()
- 10381780036302 ()
- 4 platinum contacts
- Depth electrode
The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices.
Elutia Med LLC
440579
In Commercial Distribution
- 04035479160647 ()
- 04035479160555 ()
- SubQ
- Cardiovascular patch, animal-derived
The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices.
Elutia Med LLC
440578
In Commercial Distribution
- 04035479160548 ()
- 04035479160654 ()
- Width: 9.5 Centimeter
- Height: 6.9 Centimeter
- Cardiovascular patch, animal-derived
The BioEnvelope is intended to securely hold a cardiac implantable electronic device to create a stable environment when implanted in the body. The cardiac implantable devices that may be used with the BioEnvelope include pacemaker pulse generators, defibrillators, or other cardiac implantable electronic devices.
Elutia Med LLC
440577
In Commercial Distribution
- 04035479160531 ()
- 04035479160616 ()
- Width: 8.0 Centimeter
- Height: 6.9 Centimeter
- Cardiovascular patch, animal-derived