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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-O Screw, 9.0x50mm 2S Monoaxial
Nuvasive, Inc.
13089050
In Commercial Distribution

  • 00887517551429 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x45mm 2S Monoaxial
Nuvasive, Inc.
13089045
In Commercial Distribution

  • 00887517551412 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x40mm 2S Monoaxial
Nuvasive, Inc.
13089040
In Commercial Distribution

  • 00887517551405 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x35mm 2S Monoaxial
Nuvasive, Inc.
13089035
In Commercial Distribution

  • 00887517551399 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x30mm 2S Monoaxial
Nuvasive, Inc.
13089030
In Commercial Distribution

  • 00887517551382 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x25mm 2S Monoaxial
Nuvasive, Inc.
13089025
In Commercial Distribution

  • 00887517551375 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x120mm 2S Monoaxial
Nuvasive, Inc.
13089012
In Commercial Distribution

  • 00887517551368 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x110mm 2S Monoaxial
Nuvasive, Inc.
13089011
In Commercial Distribution

  • 00887517551351 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 9.0x100mm 2S Monoaxial
Nuvasive, Inc.
13089010
In Commercial Distribution

  • 00887517551344 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 8.5x95mm 2S Monoaxial
Nuvasive, Inc.
13088595
In Commercial Distribution

  • 00887517551337 ()


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