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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 MAS Trauma Screw, 11.5x60mm Cann
Nuvasive, Inc.
16081560
In Commercial Distribution

  • 00887517558640 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x55mm Cann
Nuvasive, Inc.
16081555
In Commercial Distribution

  • 00887517558633 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x50mm Cann
Nuvasive, Inc.
16081550
In Commercial Distribution

  • 00887517558626 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x45mm Cann
Nuvasive, Inc.
16081545
In Commercial Distribution

  • 00887517558619 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x40mm Cann
Nuvasive, Inc.
16081540
In Commercial Distribution

  • 00887517558602 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS-T Screw, 11.5x35mm 2C Mono
Nuvasive, Inc.
16081535
In Commercial Distribution

  • 00887517558596 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x30mm Cann
Nuvasive, Inc.
16081530
In Commercial Distribution

  • 00887517558589 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x25mm Cann
Nuvasive, Inc.
16081525
In Commercial Distribution

  • 00887517558572 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x120mm Cann
Nuvasive, Inc.
16081512
In Commercial Distribution

  • 00887517558565 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.5x110mm Cann
Nuvasive, Inc.
16081511
In Commercial Distribution

  • 00887517558558 ()


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