SEARCH RESULTS FOR: Origin(2592 results)
Thin Wall Carotid Patch Gelatin Impregnated Thin Wall Knitted Carotid Patch TAPERED PATCH
VASCUTEK LTD
921550T
In Commercial Distribution
- 05037881010861 ()
- Dimension 15 x 50 mm
921550T
- Cardiovascular patch, animal-derived
Thin Wall Carotid Patch Gelatin Impregnated Thin Wall Knitted Carotid Patch TAPERED PATCH
VASCUTEK LTD
921010T
In Commercial Distribution
- 05037881010854 ()
- Dimension 10 x 100 mm
921010T
- Cardiovascular patch, animal-derived
Thin Wall Carotid Patch Gelatin Impregnated Thin Wall Knitted Carotid Patch TAPERED PATCH
VASCUTEK LTD
921075T
In Commercial Distribution
- 05037881010847 ()
- Dimension 10 x 75 mm
921075T
- Cardiovascular patch, animal-derived
Thin Wall Carotid Patch Gelatin Impregnated Thin Wall Knitted Carotid Patch TAPERED PATCH
VASCUTEK LTD
921050T
In Commercial Distribution
- 05037881010830 ()
- Dimension 10 x 50 mm
921050T
- Cardiovascular patch, animal-derived
Thin Wall Carotid Patch Gelatin Impregnated Thin Wall Knitted Carotid Patch TAPERED PATCH
VASCUTEK LTD
920875T
In Commercial Distribution
- 05037881010823 ()
- Dimension 8 x 75 mm
920875T
- Cardiovascular patch, animal-derived
Thin Wall Carotid Patch Gelatin Impregnated Thin Wall Knitted Carotid Patch TAPERED PATCH
VASCUTEK LTD
920675T
In Commercial Distribution
- 05037881010816 ()
- Dimension 6 x 75 mm
920675T
- Cardiovascular patch, animal-derived
Trexo Robotics XL Trexo Plus 1 Shipment
Trexo Robotics Inc.
A0001
In Commercial Distribution
- 00628719321072 ()
- XL
A001BPX
- Programmable ambulation exoskeleton, clinical
Trexo Robotics Large Trexo Plus 1 Shipment
Trexo Robotics Inc.
A0001
In Commercial Distribution
- 00628719321065 ()
- Large
A001BPR
- Programmable ambulation exoskeleton, clinical
Trexo Robotics Medium Trexo Plus 1 Shipment
Trexo Robotics Inc.
A0001
In Commercial Distribution
- 00628719321058 ()
- Medium
A001BPR
- Programmable ambulation exoskeleton, clinical
Trexo Robotics Small Trexo Plus 1 Shipment
Trexo Robotics Inc.
A0001
In Commercial Distribution
- 00628719321041 ()
- Small
A001BPR
- Programmable ambulation exoskeleton, clinical
Trumpf Medical Kit (1) VSTR08, (1) EZLINK01, (1) FS10004, (3) S-PA2010, (2) BLAP100V, (3) S-VTWT624
Conmed Corporation
TRUMPFKIT02
In Commercial Distribution
- 30845854081000 ()
TRUMPFKIT02
- Surgical plume evacuation system
Tyke is intended for use in neonates and infants for repair of pericardial structures, as an epicardial covering for damaged or repaired cardiac structures, as a patch material for intracardiac defects, septal defect and annulus repair, suture-line buttressing, and cardiac repair.
AZIYO BIOLOGICS, INC.
CMCV-098-204
In Commercial Distribution
- 10859389005109 ()
- 00859389005102 ()
- Height: 4 Centimeter
- Width: 7 Centimeter
- Cardiovascular patch, animal-derived
No Description
I.C. MEDICAL, INC.
ICM-000-0460
In Commercial Distribution
- 00817688021780 ()
- 00817688021773 ()
- Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
ICM-000-0289
In Commercial Distribution
- 00817688021681 ()
- 00817688021674 ()
- Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
ICM-000-0276
In Commercial Distribution
- 00817688021667 ()
- 00817688021650 ()
- Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
ICM-000-0262
In Commercial Distribution
- 00817688021643 ()
- 00817688021636 ()
- Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
2210
Not in Commercial Distribution
- 00817688021483 ()
- 00817688021476 ()
ICM-000-0420
- Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
ICM-000-0307
Not in Commercial Distribution
- 00817688021469 ()
- 00817688021452 ()
- Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
ICM-000-0014
In Commercial Distribution
- 00817688021445 ()
- 00817688021438 ()
- Surgical plume evacuation system
UNIVERSAL BLUE™ RF Sensor
I.C. MEDICAL, INC.
ICM-000-0599
In Commercial Distribution
- 00817688020363 ()
ICM-000-0599
- Surgical plume evacuation system
Unloading harness for gait training
M.A.S.S. Rehab, LLC
Standard
In Commercial Distribution
- G505MRUHS0 ()
- Gait rehabilitation system harness
Bariatric Harness for persons 300-600 lbs
M.A.S.S. Rehab, LLC
Bariatric
In Commercial Distribution
- G505MRUHB0 ()
- Gait rehabilitation system harness
VASCU-GUARD Peripheral Vascular Patch is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. VASCU-GUARD Peripheral Vascular Patch is chemically sterilized using ethanol and propylene oxide. VASCU-GUARD Peripheral Vascular Patch has been treated with 1 molar sodium hydroxide for a minimum of 60 minutes at 20 - 25°C. VASCU-GUARD Peripheral Vascular Patch is packaged in a container filled with sterile, non-pyrogenic water containing propylene oxide. The contents of the unopened, undamaged container are sterile.
SYNOVIS LIFE TECHNOLOGIES, INC.
VG0209N
In Commercial Distribution
- 00085412530925 ()
VG0209N
- Cardiovascular patch, animal-derived
VASCU-GUARD Peripheral Vascular Patch is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. VASCU-GUARD Peripheral Vascular Patch is chemically sterilized using ethanol and propylene oxide. VASCU-GUARD Peripheral Vascular Patch has been treated with 1 molar sodium hydroxide for a minimum of 60 minutes at 20 - 25°C. VASCU-GUARD Peripheral Vascular Patch is packaged in a container filled with sterile, non-pyrogenic water containing propylene oxide. The contents of the unopened, undamaged container are sterile.
SYNOVIS LIFE TECHNOLOGIES, INC.
VG0110N
In Commercial Distribution
- 00085412530918 ()
VG0110N
- Cardiovascular patch, animal-derived
VASCU-GUARD Peripheral Vascular Patch is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. VASCU-GUARD Peripheral Vascular Patch is chemically sterilized using ethanol and propylene oxide. VASCU-GUARD Peripheral Vascular Patch has been treated with 1 molar sodium hydroxide for a minimum of 60 minutes at 20 - 25°C. VASCU-GUARD Peripheral Vascular Patch is packaged in a container filled with sterile, non-pyrogenic water containing propylene oxide. The contents of the unopened, undamaged container are sterile.
SYNOVIS LIFE TECHNOLOGIES, INC.
VG0108N
In Commercial Distribution
- 00085412530895 ()
VG0108N
- Cardiovascular patch, animal-derived
VASCU-GUARD Peripheral Vascular Patch is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. VASCU-GUARD Peripheral Vascular Patch is chemically sterilized using ethanol and propylene oxide. VASCU-GUARD Peripheral Vascular Patch has been treated with 1 molar sodium hydroxide for a minimum of 60 minutes at 20 - 25 C. VASCU-GUARD Peripheral Vascular Patch is packaged in a container filled with sterile, non-pyrogenic water containing propylene oxide. The contents of the unopened, undamaged container are sterile.
SYNOVIS LIFE TECHNOLOGIES, INC.
VG0106N
In Commercial Distribution
- 00085412530871 ()
VG0106N
- Cardiovascular patch, animal-derived
ViroSafe VisiClear Filter Smoke Evacuation Filter 3-port - 1/4 in (6.4mm), 3/8 in (9.5mm), and 7/8 in (22mm)
Conmed Corporation
VV220
In Commercial Distribution
- 20845854081317 ()
VV220
- Surgical plume evacuation system
ViroVac Surgical Smoke Evacuator with Filter 100V-120V 50/60Hz
Conmed Corporation
VV120
VV120
- Surgical plume evacuation system
ViroVac Surgical Smoke Evacuator 100V-120V 50/60Hz
Conmed Corporation
VV120NF
VV120NF
- Surgical plume evacuation system
VIROVAC SMOKE EVACUATION SYSTEM WITH VIROSAFE 3-PORT FILTER 220V-240V 50/60HZ
Conmed Corporation
ASVV220
In Commercial Distribution
- 30845854648685 ()
ASVV220
- Surgical plume evacuation system
ViroVac Wall Mount Kit
Conmed Corporation
VVWM01
VVWM01
- Surgical plume evacuation system
ViroVac Surgical Smoke Evacuator with Filter 220V-240V 50/60Hz
Conmed Corporation
DKVV220
In Commercial Distribution
- 30845854081765 ()
DKVV220
- Surgical plume evacuation system
VisiClear Surgical Smoke Evacuator with Filter 220V-240V 50/60 Hz
Conmed Corporation
VC220P1
Not in Commercial Distribution
- 20845854081355 ()
VC220P1
- Surgical plume evacuation system
VisiClear Surgical Smoke Evacuator 220V-240V 50/60Hz
Conmed Corporation
VC220NF
Not in Commercial Distribution
- 20845854081348 ()
VC220NF
- Surgical plume evacuation system
VisiClear Surgical Smoke Evacuator with Filter 220V-240V 50/60 Hz
Conmed Corporation
VC220
In Commercial Distribution
- 20845854081324 ()
VC220
- Surgical plume evacuation system
VisiClear Surgical Smoke Evacuator with Filter 100V-120V 50/60 Hz
Conmed Corporation
VC120
VC120
- Surgical plume evacuation system
VisiClear Surgical Smoke Evacuator 100V-120V 50/60 Hz
Conmed Corporation
VC120NF
VC120NF
- Surgical plume evacuation system
The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-L is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-L is designed to be implanted bi-laterally via posterior (PLIF) approach or as a single device via a transverse (TLIF) approach. VariLift-L may be implanted with or without supplemental fixation and is intended for use with autograft to facilitate fusion. VariLift-L is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment. The device is intended for use at either one level or two contiguous levels for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.
Wenzel Spine, Inc.
CIE2-15-24-00
In Commercial Distribution
- 00813210020023 ()
- Length: 24 Millimeter
- Outer Diameter: 15 Millimeter
- Metallic spinal interbody fusion cage
The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-L is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-L is designed to be implanted bi-laterally via posterior (PLIF) approach or as a single device via a transverse (TLIF) approach. VariLift-L may be implanted with or without supplemental fixation and is intended for use with autograft to facilitate fusion. VariLift-L is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment. The device is intended for use at either one level or two contiguous levels for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.
Wenzel Spine, Inc.
CIE2-13-24-00
In Commercial Distribution
- 00813210020016 ()
- Length: 24 Millimeter
- Outer Diameter: 13 Millimeter
- Metallic spinal interbody fusion cage
The Wenzel Spine VariLift Lumbar Interbody Fusion Device is a self-tapping, expandable device with an interior sliding wedge and a posterior end cap. The VariLift-L is a grooved and fluted device with large graft windows positioned each of its four quadrants that provide bony contact with the endplates. VariLift-L is designed to be implanted bi-laterally via posterior (PLIF) approach or as a single device via a transverse (TLIF) approach. VariLift-L may be implanted with or without supplemental fixation and is intended for use with autograft to facilitate fusion. VariLift-L is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment. The device is intended for use at either one level or two contiguous levels for the treatment of degenerative disc disease (DDD) with up to Grade 1 spondylolisthesis. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies.
Wenzel Spine, Inc.
CIE2-11-24-00
In Commercial Distribution
- 00813210020009 ()
- Length: 24 Millimeter
- Outer Diameter: 11 Millimeter
- Metallic spinal interbody fusion cage