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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, 10.0x95mm 2S Reduction
Nuvasive, Inc.
13021095
In Commercial Distribution

  • 00887517538758 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x90mm 2S Reduction
Nuvasive, Inc.
13021090
In Commercial Distribution

  • 00887517538741 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x85mm 2S Reduction
Nuvasive, Inc.
13021085
In Commercial Distribution

  • 00887517538734 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x80mm 2S Reduction
Nuvasive, Inc.
13021080
In Commercial Distribution

  • 00887517538727 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x75mm 2S Reduction
Nuvasive, Inc.
13021075
In Commercial Distribution

  • 00887517538710 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x70mm 2S Reduction
Nuvasive, Inc.
13021070
In Commercial Distribution

  • 00887517538703 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x65mm 2S Reduction
Nuvasive, Inc.
13021065
In Commercial Distribution

  • 00887517538697 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x60mm 2S Reduction
Nuvasive, Inc.
13021060
In Commercial Distribution

  • 00887517538680 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x55mm 2S Reduction
Nuvasive, Inc.
13021055
In Commercial Distribution

  • 00887517538673 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 10.0x50mm 2S Reduction
Nuvasive, Inc.
13021050
In Commercial Distribution

  • 00887517538666 ()


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