Company Name Brand Name GMDN Term Name GMDN Term Status 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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FORTIFY I -R 14mm Upper Endplate, 14x14mm Footprint, 3.5°, No Spikes
GLOBUS MEDICAL, INC.
337.301
In Commercial Distribution

  • 00889095215991 ()

  • Depth: 14 Millimeter
  • Sagittal Profile 3.5 Degree
  • Width: 14 Millimeter


  • Vertebral body prosthesis
FORTIFY I -R 14mm Upper Endplate, 14x14mm Footprint, 0°, No Spikes
GLOBUS MEDICAL, INC.
337.300
In Commercial Distribution

  • 00889095215984 ()

  • Depth: 14 Millimeter
  • Width: 14 Millimeter


  • Vertebral body prosthesis
FORTIFY I 12mm Core, Height 23-28mm,12x14mm Footprint, 7&deg, No Spikes
GLOBUS MEDICAL, INC.
137.003
In Commercial Distribution

  • 00889095040791 ()

  • Width: 14 Millimeter
  • Sagittal Profile 7 Degree
  • Depth: 12 Millimeter
  • Height: 23 Millimeter


  • Vertebral body prosthesis
FORTIFY I 12mm Core, Height 23-28mm,12x14mm Footprint, 3.5&deg, No Spikes
GLOBUS MEDICAL, INC.
137.002
In Commercial Distribution

  • 00889095040784 ()

  • Depth: 12 Millimeter
  • Sagittal Profile 3.5 Degree
  • Width: 14 Millimeter
  • Height: 23 Millimeter


  • Vertebral body prosthesis
FORTIFY I 12mm Core, Height 23-28mm,12x14mm Footprint, 0&deg, No Spikes
GLOBUS MEDICAL, INC.
137.001
In Commercial Distribution

  • 00889095040777 ()

  • Width: 14 Millimeter
  • Height: 23 Millimeter
  • Depth: 12 Millimeter


  • Vertebral body prosthesis
P I ARROWg+ard Blue Plus(R) Quad-Lumen Central Venous Catheterization Kit
TELEFLEX INCORPORATED
IPN037295
In Commercial Distribution

  • 20801902113584 ()
  • 10801902113587 ()
ASK-42854-POHU

  • Centrally-inserted central venous catheter
P I ARROWg+ard Blue Plus(R) Quad-Lumen Central Venous Catheterization Kit
TELEFLEX INCORPORATED
IPN035041
In Commercial Distribution

  • 20801902113577 ()
  • 10801902113570 ()
ASK-42854-POHU

  • Centrally-inserted central venous catheter
Bone Graft Substitute, Foam Pack, Beta-Tricalcium Phosphate and Type I Bovine Collagen
Stryker Corporation
2102-1410
In Commercial Distribution

  • 00808232000443 ()

  • Total Volume: 10.0 Cubic Centimeter
2102-1410

  • Bone matrix implant, composite
Bone Graft Substitute, Foam Pack, Beta-Tricalcium Phosphate and Type I Bovine Collagen
Stryker Corporation
2102-1405
In Commercial Distribution

  • 00808232000436 ()

  • Total Volume: 5.0 Cubic Centimeter
2102-1405

  • Bone matrix implant, composite
Bone Graft Substitute, Foam Pack, Beta-Tricalcium Phosphate and Type I Bovine Collagen
Stryker Corporation
2102-1402
In Commercial Distribution

  • 00808232000429 ()

  • Total Volume: 2.5 Cubic Centimeter
2102-1402

  • Bone matrix implant, composite
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