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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 Ti Rod, 5.5x65mm Lordotic
Nuvasive, Inc.
14355065P
In Commercial Distribution

  • 00887517040978 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Ti Rod, 5.5x60mm Lordotic
Nuvasive, Inc.
14355060P
In Commercial Distribution

  • 00887517040961 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Ti Rod, 5.5x55mm Lordotic
Nuvasive, Inc.
14355055P
In Commercial Distribution

  • 00887517040954 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Ti Rod, 5.5x50mm Lordotic
Nuvasive, Inc.
14355050P
In Commercial Distribution

  • 00887517040947 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Ti Rod, 5.5x40mm Lordotic
Nuvasive, Inc.
14355040P
In Commercial Distribution

  • 00887517040923 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE-O Ti Rod, 5.5x30mm Lordotic
Nuvasive, Inc.
14355030P
In Commercial Distribution

  • 00887517040909 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE Screw+LS, 8.5x55mm 2FS Poly
Nuvasive, Inc.
14118555P
In Commercial Distribution

  • 00887517040886 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE Screw+LS, 8.5x50mm 2FS Poly
Nuvasive, Inc.
14118550P
In Commercial Distribution

  • 00887517040879 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE Screw+LS, 8.5x40mm 2FS Poly
Nuvasive, Inc.
14118540P
In Commercial Distribution

  • 00887517040855 ()


  • Bone-screw internal spinal fixation system, sterile
RELINE Screw+LS, 7.5x50mm 2FS Poly
Nuvasive, Inc.
14117550P
In Commercial Distribution

  • 00887517040831 ()


  • Bone-screw internal spinal fixation system, sterile
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