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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, 7.0x90mm Cann
Nuvasive, Inc.
16087090
In Commercial Distribution

  • 00887517559968 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x85mm Cann
Nuvasive, Inc.
16087085
In Commercial Distribution

  • 00887517559951 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x80mm Cann
Nuvasive, Inc.
16087080
In Commercial Distribution

  • 00887517559944 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x75mm Cann
Nuvasive, Inc.
16087075
In Commercial Distribution

  • 00887517559937 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x70mm Cann
Nuvasive, Inc.
16087070
In Commercial Distribution

  • 00887517559920 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x65mm Cann
Nuvasive, Inc.
16087065
In Commercial Distribution

  • 00887517559913 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x60mm Cann
Nuvasive, Inc.
16087060
In Commercial Distribution

  • 00887517559906 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x55mm Cann
Nuvasive, Inc.
16087055
In Commercial Distribution

  • 00887517559890 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x50mm Cann
Nuvasive, Inc.
16087050
In Commercial Distribution

  • 00887517559883 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE MAS Trauma Screw, 7.0x45mm Cann
Nuvasive, Inc.
16087045
In Commercial Distribution

  • 00887517559876 ()


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