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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-ONE Shank, 4.5x65mm 2FC MOD FEN
Nuvasive, Inc.
24034565
In Commercial Distribution

  • 00195377090041 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 4.5x60mm 2FC MOD FEN
Nuvasive, Inc.
24034560
In Commercial Distribution

  • 00195377090034 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 4.5x55mm 2FC MOD FEN
Nuvasive, Inc.
24034555
In Commercial Distribution

  • 00195377090027 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 4.5x50mm 2FC MOD FEN
Nuvasive, Inc.
24034550
In Commercial Distribution

  • 00195377090010 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 4.5x45mm 2FC MOD FEN
Nuvasive, Inc.
24034545
In Commercial Distribution

  • 00195377090003 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 4.5x40mm 2FC MOD FEN
Nuvasive, Inc.
24034540
In Commercial Distribution

  • 00195377089991 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 4.5x35mm 2FC MOD FEN
Nuvasive, Inc.
24034535
In Commercial Distribution

  • 00195377089984 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 4.5x30mm 2FC MOD FEN
Nuvasive, Inc.
24034530
In Commercial Distribution

  • 00195377089977 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 10.0x95mm 2FC MOD FEN
Nuvasive, Inc.
24031095
In Commercial Distribution

  • 00195377089953 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-ONE Shank, 10.0x90mm 2FC MOD FEN
Nuvasive, Inc.
24031090
In Commercial Distribution

  • 00195377089946 ()


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