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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 Size Type Device Class Implantable

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RELINE-O Screw, 4.0x35mm 2S Reduction
Nuvasive, Inc.
13024035
In Commercial Distribution

  • 00887517539533 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x30mm 2S Reduction
Nuvasive, Inc.
13024030
In Commercial Distribution

  • 00887517539526 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x25mm 2S Reduction
Nuvasive, Inc.
13024025
In Commercial Distribution

  • 00887517539519 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x120mm 2S Reduction
Nuvasive, Inc.
13024012
In Commercial Distribution

  • 00887517539502 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x110mm 2S Reduction
Nuvasive, Inc.
13024011
In Commercial Distribution

  • 00887517539496 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x100mm 2S Reduction
Nuvasive, Inc.
13024010
In Commercial Distribution

  • 00887517539489 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x95mm 2S Reduction
Nuvasive, Inc.
13022595
In Commercial Distribution

  • 00887517539472 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x90mm 2S Reduction
Nuvasive, Inc.
13022590
In Commercial Distribution

  • 00887517539465 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x85mm 2S Reduction
Nuvasive, Inc.
13022585
In Commercial Distribution

  • 00887517539458 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x80mm 2S Reduction
Nuvasive, Inc.
13022580
In Commercial Distribution

  • 00887517539441 ()


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