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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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SHANK PK 55902507535 ST MX OG 7.5X35 2PK
MEDTRONIC SOFAMOR DANEK, INC.
55902507535
In Commercial Distribution

  • 20763000607306 ()
  • 00763000607302 ()


  • Bone-screw internal spinal fixation system, sterile
SHANK PK 55902508550 ST MX OG 8.5X50 2PK
MEDTRONIC SOFAMOR DANEK, INC.
55902508550
In Commercial Distribution

  • 20763000713038 ()
  • 00763000713034 ()


  • Bone-screw internal spinal fixation system, sterile
SHANK PK 55902508545 ST MX OG 8.5X45 2PK
MEDTRONIC SOFAMOR DANEK, INC.
55902508545
In Commercial Distribution

  • 20763000713021 ()
  • 00763000713027 ()


  • Bone-screw internal spinal fixation system, sterile
SHANK PK 55902508540 ST MX OG 8.5X40 2PK
MEDTRONIC SOFAMOR DANEK, INC.
55902508540
In Commercial Distribution

  • 20763000713014 ()
  • 00763000713010 ()


  • Bone-screw internal spinal fixation system, sterile
No Description
ZIMMER SPINE, INC.
07.01797.002
In Commercial Distribution

  • 00889024329164 ()
07.01797.002

  • Bone tap, reusable
No Description
ZIMMER BIOMET INC
07.01797.001
In Commercial Distribution

  • 00889024329157 ()
07.01797.001

  • Bone tap, reusable
No Description
ZIMMER SPINE, INC.
07.01796.002
In Commercial Distribution

  • 00889024329140 ()
07.01796.002

  • Bone tap, reusable
No Description
ZIMMER BIOMET INC
07.01796.001
In Commercial Distribution

  • 00889024329133 ()
07.01796.001

  • Bone tap, reusable
No Description
ZIMMER SPINE, INC.
07.01793.003
In Commercial Distribution

  • 00889024329126 ()
07.01793.003

  • Spinal implant trial
No Description
ZIMMER BIOMET INC
07.01793.002
In Commercial Distribution

  • 00889024329119 ()
07.01793.002

  • Spinal implant trial
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