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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 Class Implantable

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RELINE-O Screw+LS, 7.5x30mm 2S Mono
Nuvasive, Inc.
13387530P
In Commercial Distribution

  • 00887517040619 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x55mm 2S Mono
Nuvasive, Inc.
13386555P
In Commercial Distribution

  • 00887517040602 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x50mm 2S Mono
Nuvasive, Inc.
13386550P
In Commercial Distribution

  • 00887517040596 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x45mm 2S Mono
Nuvasive, Inc.
13386545P
In Commercial Distribution

  • 00887517040589 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x40mm 2S Mono
Nuvasive, Inc.
13386540P
In Commercial Distribution

  • 00887517040572 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x35mm 2S Mono
Nuvasive, Inc.
13386535P
In Commercial Distribution

  • 00887517040565 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 6.5x30mm 2S Mono
Nuvasive, Inc.
13386530P
In Commercial Distribution

  • 00887517040558 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 5.5x55mm 2S Mono
Nuvasive, Inc.
13385555P
In Commercial Distribution

  • 00887517040541 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 5.5x50mm 2S Mono
Nuvasive, Inc.
13385550P
In Commercial Distribution

  • 00887517040534 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Screw+LS, 5.5x45mm 2S Mono
Nuvasive, Inc.
13385545P
In Commercial Distribution

  • 00887517040527 ()


  • Bone-screw internal spinal fixation system, sterile
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