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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 Class Implantable

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RELINE Screw, 8.5x50mm 2FC Polyaxial
Nuvasive, Inc.
16218550
In Commercial Distribution

  • 00887517924568 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.5x45mm 2FC Polyaxial
Nuvasive, Inc.
16218545
In Commercial Distribution

  • 00887517924551 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.5x40mm 2FC Polyaxial
Nuvasive, Inc.
16218540
In Commercial Distribution

  • 00887517924544 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.5x35mm 2FC Polyaxial
Nuvasive, Inc.
16218535
In Commercial Distribution

  • 00887517924537 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.5x30mm 2FC Polyaxial
Nuvasive, Inc.
16218530
In Commercial Distribution

  • 00887517924520 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.5x100mm 2FC Polyaxial
Nuvasive, Inc.
16218510
In Commercial Distribution

  • 00887517924490 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.0x95mm 2FC Polyaxial
Nuvasive, Inc.
16218095
In Commercial Distribution

  • 00887517924483 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.0x90mm 2FC Polyaxial
Nuvasive, Inc.
16218090
In Commercial Distribution

  • 00887517924476 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.0x85mm 2FC Polyaxial
Nuvasive, Inc.
16218085
In Commercial Distribution

  • 00887517924469 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE Screw, 8.0x80mm 2FC Polyaxial
Nuvasive, Inc.
16218080
In Commercial Distribution

  • 00887517924452 ()


  • Bone-screw internal spinal fixation system, non-sterile
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