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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, 11.0x70mm Cann
Nuvasive, Inc.
16081170
In Commercial Distribution

  • 00887517558305 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x65mm Cann
Nuvasive, Inc.
16081165
In Commercial Distribution

  • 00887517558299 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x60mm Cann
Nuvasive, Inc.
16081160
In Commercial Distribution

  • 00887517558282 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x55mm Cann
Nuvasive, Inc.
16081155
In Commercial Distribution

  • 00887517558275 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x50mm Cann
Nuvasive, Inc.
16081150
In Commercial Distribution

  • 00887517558268 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x45mm Cann
Nuvasive, Inc.
16081145
In Commercial Distribution

  • 00887517558251 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x40mm Cann
Nuvasive, Inc.
16081140
In Commercial Distribution

  • 00887517558244 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x35mm Cann
Nuvasive, Inc.
16081135
In Commercial Distribution

  • 00887517558237 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x30mm Cann
Nuvasive, Inc.
16081130
In Commercial Distribution

  • 00887517558220 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 11.0x25mm Cann
Nuvasive, Inc.
16081125
In Commercial Distribution

  • 00887517558213 ()


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