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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, 12.0x65mm 2S Reduction
Nuvasive, Inc.
13021265
In Commercial Distribution

  • 00887517539052 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x60mm 2S Reduction
Nuvasive, Inc.
13021260
In Commercial Distribution

  • 00887517539045 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x55mm 2S Reduction
Nuvasive, Inc.
13021255
In Commercial Distribution

  • 00887517539038 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x50mm 2S Reduction
Nuvasive, Inc.
13021250
In Commercial Distribution

  • 00887517539021 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x45mm 2S Reduction
Nuvasive, Inc.
13021245
In Commercial Distribution

  • 00887517539014 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x40mm 2S Reduction
Nuvasive, Inc.
13021240
In Commercial Distribution

  • 00887517539007 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x35mm 2S Reduction
Nuvasive, Inc.
13021235
In Commercial Distribution

  • 00887517538994 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x30mm 2S Reduction
Nuvasive, Inc.
13021230
In Commercial Distribution

  • 00887517538987 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x25mm 2S Reduction
Nuvasive, Inc.
13021225
In Commercial Distribution

  • 00887517538970 ()


  • Bone-screw internal spinal fixation system, non-sterile
RELINE-O Screw, 12.0x120mm 2S Reduction
Nuvasive, Inc.
13021212
In Commercial Distribution

  • 00887517538963 ()


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