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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, 4.0x75mm 2S Reduction
Nuvasive, Inc.
13024075
In Commercial Distribution

  • 00887517539618 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x60mm 2S Reduction
Nuvasive, Inc.
13024060
In Commercial Distribution

  • 00887517539588 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x55mm 2S Reduction
Nuvasive, Inc.
13024055
In Commercial Distribution

  • 00887517539571 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 4.0x45mm 2S Reduction
Nuvasive, Inc.
13024045
In Commercial Distribution

  • 00887517539557 ()


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

  • 00887517539519 ()


  • 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, 12.5x85mm 2S Reduction
Nuvasive, Inc.
13022585
In Commercial Distribution

  • 00887517539458 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x75mm 2S Reduction
Nuvasive, Inc.
13022575
In Commercial Distribution

  • 00887517539434 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.5x65mm 2S Reduction
Nuvasive, Inc.
13022565
In Commercial Distribution

  • 00887517539410 ()


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