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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 Class Implantable

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RELINE-O Screw, 6.0x70mm 2S Monoaxial
Nuvasive, Inc.
13086070
In Commercial Distribution

  • 00887517550385 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x60mm 2S Monoaxial
Nuvasive, Inc.
13086060
In Commercial Distribution

  • 00887517550361 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x50mm 2S Monoaxial
Nuvasive, Inc.
13086050
In Commercial Distribution

  • 00887517550347 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x45mm 2S Monoaxial
Nuvasive, Inc.
13086045
In Commercial Distribution

  • 00887517550330 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x35mm 2S Monoaxial
Nuvasive, Inc.
13086035
In Commercial Distribution

  • 00887517550316 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x25mm 2S Monoaxial
Nuvasive, Inc.
13086025
In Commercial Distribution

  • 00887517550293 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x110mm 2S Monoaxial
Nuvasive, Inc.
13086011
In Commercial Distribution

  • 00887517550279 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 6.0x100mm 2S Monoaxial
Nuvasive, Inc.
13086010
In Commercial Distribution

  • 00887517550262 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x90mm 2S Monoaxial
Nuvasive, Inc.
13085590
In Commercial Distribution

  • 00887517550248 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 5.5x75mm 2S Monoaxial
Nuvasive, Inc.
13085575
In Commercial Distribution

  • 00887517550217 ()


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