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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, 8.0x70mm Cann
Nuvasive, Inc.
16088070
In Commercial Distribution

  • 00887517560285 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x65mm Cann
Nuvasive, Inc.
16088065
In Commercial Distribution

  • 00887517560278 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x60mm Cann
Nuvasive, Inc.
16088060
In Commercial Distribution

  • 00887517560261 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x55mm Cann
Nuvasive, Inc.
16088055
In Commercial Distribution

  • 00887517560254 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x50mm Cann
Nuvasive, Inc.
16088050
In Commercial Distribution

  • 00887517560247 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x45mm Cann
Nuvasive, Inc.
16088045
In Commercial Distribution

  • 00887517560230 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x40mm Cann
Nuvasive, Inc.
16088040
In Commercial Distribution

  • 00887517560223 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x35mm Cann
Nuvasive, Inc.
16088035
In Commercial Distribution

  • 00887517560216 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x30mm Cann
Nuvasive, Inc.
16088030
In Commercial Distribution

  • 00887517560209 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 8.0x25mm Cann
Nuvasive, Inc.
16088025
In Commercial Distribution

  • 00887517560193 ()


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