Company Name Brand Name GMDN Term FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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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.
CIE2-11-24-00
In Commercial Distribution

  • 00813210020009 ()

  • Length: 24 Millimeter
  • Outer Diameter: 11 Millimeter


  • Metallic spinal interbody fusion cage
VisiClear Surgical Smoke Evacuator with Filter 100V-120V 50/60 Hz
Conmed Corporation
VC120
In Commercial Distribution

  • 30845854081970 ()
VC120

  • Surgical plume evacuation system
VisiClear Surgical Smoke Evacuator 100V-120V 50/60 Hz
Conmed Corporation
VC120NF
In Commercial Distribution

  • 10845854081976 ()
  • 30845854081963 ()
VC120NF

  • Surgical plume evacuation system
VisiClear Surgical Smoke Evacuator with Filter 220V-240V 50/60 Hz
Conmed Corporation
VC220P1
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
ViroVac Surgical Smoke Evacuator with Filter 100V-120V 50/60Hz
Conmed Corporation
VV120
In Commercial Distribution

  • 10845854081969 ()
  • 30845854081956 ()
VV120

  • Surgical plume evacuation system
ViroVac Surgical Smoke Evacuator 100V-120V 50/60Hz
Conmed Corporation
VV120NF
In Commercial Distribution

  • 10845854081952 ()
  • 30845854081949 ()
VV120NF

  • Surgical plume evacuation system
ViroVac Wall Mount Kit
Conmed Corporation
VVWM01
In Commercial Distribution

  • 30845854081888 ()
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
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
No Description
U&I CORPORATION
PE1020
In Commercial Distribution

  • 08800015953986 ()


  • Bone graft packing block
Vascu-Guard is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Vascu-Guard is chemically sterilized using ethanol and propylene oxide. Vascu-Guard has been treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C. Vascu-Guard 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 is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Vascu-Guard is chemically sterilized using ethanol and propylene oxide. Vascu-Guard has been treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C. Vascu-Guard 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 is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Vascu-Guard is chemically sterilized using ethanol and propylene oxide. Vascu-Guard has been treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C. Vascu-Guard 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 is prepared from bovine pericardium which is cross-linked with glutaraldehyde. The pericardium is procured from cattle originating in the United States. Vascu-Guard is chemically sterilized using ethanol and propylene oxide. Vascu-Guard has been treated with 1 molar sodium hydroxide for 60-75 minutes at 20-25C. Vascu-Guard 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
SIJ Bone Graft Packing Instrument
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08800039822183 ()
SI.IN.0031

  • Bone graft packing block
UNIVERSAL BLUE™ RF Sensor
I.C. MEDICAL, INC.
ICM-000-0599
In Commercial Distribution

  • 00817688020363 ()
ICM-000-0599

  • Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
2210
In Commercial Distribution

  • 00817688021483 ()
  • 00817688021476 ()
ICM-000-0420

  • Surgical plume evacuation system
No Description
I.C. MEDICAL, INC.
ICM-000-0307
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
Ulpa Filter w/fluid Trap, Mega Vac Smoke Evacuator, Non-sterile
MEGADYNE MEDICAL PRODUCTS, INC.
2211J
In Commercial Distribution

  • 30614559105416 ()
  • 10614559105412 ()


  • Surgical plume evacuation system
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
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
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
Iris Straight Bipolar Forcep 3 1/2" (88.9mm) Insulated With A (High Polished 10mm Long Area) With A 0.5mm Tip Country Of Origin USA
TITAN MANUFACTURING INC
160818205030101
In Commercial Distribution

  • 00817914024905 ()


  • Open-surgery electrosurgical handpiece/electrode, bipolar, reusable
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