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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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Gradient Plate, 24mm 1-Level
Nuvasive, Inc.
7440124
In Commercial Distribution

  • 00887517479853 ()


  • Spinal fixation plate, non-bioabsorbable
SpheRx DBR II Screw, 8.5x50mm Polyaxial
Nuvasive, Inc.
7378550
In Commercial Distribution

  • 00887517479488 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx DBR II Screw, 8.5x30mm Polyaxial
Nuvasive, Inc.
7378530
In Commercial Distribution

  • 00887517479440 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx II DBR II Screw, 7.5x65mm Poly
Nuvasive, Inc.
7377565
In Commercial Distribution

  • 00887517479426 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx®II DBR®II Screw, 7.5x60mm Poly
Nuvasive, Inc.
7377560
In Commercial Distribution

  • 00887517479419 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR®II Screw, 7.5x40mm Cann Poly
Nuvasive, Inc.
7377540
In Commercial Distribution

  • 00887517479273 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx®II DBR®II Screw, 6.5x60mm Poly
Nuvasive, Inc.
7376560
In Commercial Distribution

  • 00887517479235 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR®II Screw, 6.5x55mm Cann Poly
Nuvasive, Inc.
7376555
In Commercial Distribution

  • 00887517479228 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR®II Screw, 6.5x50mm Cann Poly
Nuvasive, Inc.
7376550
In Commercial Distribution

  • 00887517479211 ()


  • Bone-screw internal spinal fixation system, non-sterile
SpheRx® DBR®II Screw, 6.5x45mm Cann Poly
Nuvasive, Inc.
7376545
In Commercial Distribution

  • 00887517479204 ()


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