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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 Class Implantable

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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
RELINE MAS Trauma Screw, 11.5x100mm Cann
Nuvasive, Inc.
16081510
In Commercial Distribution

  • 00887517558541 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 12.0x95mm Cann
Nuvasive, Inc.
16081295
In Commercial Distribution

  • 00887517558534 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 12.0x90mm Cann
Nuvasive, Inc.
16081290
In Commercial Distribution

  • 00887517558527 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 12.0x85mm Cann
Nuvasive, Inc.
16081285
In Commercial Distribution

  • 00887517558510 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 12.0x80mm Cann
Nuvasive, Inc.
16081280
In Commercial Distribution

  • 00887517558503 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 12.0x75mm Cann
Nuvasive, Inc.
16081275
In Commercial Distribution

  • 00887517558497 ()


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