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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-ONE Screw, 8.0x25mm 2C Polyaxial
Nuvasive, Inc.
24028025
In Commercial Distribution

  • 00195377088949 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 8.0x120mm 2C Polyaxial
Nuvasive, Inc.
24028012
In Commercial Distribution

  • 00195377088925 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x95mm 2C Polyaxial
Nuvasive, Inc.
24027595
In Commercial Distribution

  • 00195377088895 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x85mm 2C Polyaxial
Nuvasive, Inc.
24027585
In Commercial Distribution

  • 00195377088871 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x80mm 2C Polyaxial
Nuvasive, Inc.
24027580
In Commercial Distribution

  • 00195377088864 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x70mm 2C Polyaxial
Nuvasive, Inc.
24027570
In Commercial Distribution

  • 00195377088840 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x65mm 2C Polyaxial
Nuvasive, Inc.
24027565
In Commercial Distribution

  • 00195377088833 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x60mm 2C Polyaxial
Nuvasive, Inc.
24027560
In Commercial Distribution

  • 00195377088826 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x30mm 2C Polyaxial
Nuvasive, Inc.
24027530
In Commercial Distribution

  • 00195377088819 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Screw, 7.5x25mm 2C Polyaxial
Nuvasive, Inc.
24027525
In Commercial Distribution

  • 00195377088802 ()


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