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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+LS, 4.0x35mm 2S Mono
Nuvasive, Inc.
13384035P
In Commercial Distribution

  • 00887517040404 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 7.5x50mm 2S PLS
Nuvasive, Inc.
13367550P
In Commercial Distribution

  • 00887517040374 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 7.5x40mm 2S PLS
Nuvasive, Inc.
13367540P
In Commercial Distribution

  • 00887517040350 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 7.5x35mm 2S PLS
Nuvasive, Inc.
13367535P
In Commercial Distribution

  • 00887517040343 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x50mm 2S PLS
Nuvasive, Inc.
13366550P
In Commercial Distribution

  • 00887517040336 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x40mm 2S PLS
Nuvasive, Inc.
13366540P
In Commercial Distribution

  • 00887517040312 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x30mm 2S PLS
Nuvasive, Inc.
13366530P
In Commercial Distribution

  • 00887517040299 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 5.5x50mm 2S PLS
Nuvasive, Inc.
13365550P
In Commercial Distribution

  • 00887517040282 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 5.5x45mm 2S PLS
Nuvasive, Inc.
13365545P
In Commercial Distribution

  • 00887517040275 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 5.5x40mm 2S PLS
Nuvasive, Inc.
13365540P
In Commercial Distribution

  • 00887517040268 ()


  • Bone-screw internal spinal fixation system, sterile
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