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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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Titanium pre-bent longitudinal rod
SpineArt SA
MIS-RT 11 10-S
In Commercial Distribution

  • 07640178981966 ()

  • Length: 110 Millimeter
  • Outer Diameter: 5.4 Millimeter
MIS-RT 11 10-S

  • Bone-screw internal spinal fixation system, sterile
PEDICLE PROBE LENKE STRAIGHT
SpineArt SA
ELL-IN 02 26-N
In Commercial Distribution

  • 07640178981959 ()
ELL-IN 02 26-N

  • Bone awl, reusable
PEDICLE PROBE LENKE CURVED
SpineArt SA
ELL-IN 02 25-N
In Commercial Distribution

  • 07640178981942 ()
ELL-IN 02 25-N

  • Bone awl, reusable
PEDICLE PROBE STRAIGHT
SpineArt SA
ELL-IN 02 24-N
In Commercial Distribution

  • 07640178981935 ()
ELL-IN 02 24-N

  • Bone awl, reusable
DEROTATION HANDLE
SpineArt SA
SPE-IN 01 80-N
In Commercial Distribution

  • 07640178981928 ()
SPE-IN 01 80-N

  • Surgical instrument handle, non-torque-limiting
PERCUTANEOUS PRE-BENT ROD
SpineArt SA
MIS-RT 11 30-N
In Commercial Distribution

  • 07640178981904 ()

  • Length: 130 Millimeter
  • Outer Diameter: 5.4 Millimeter
MIS-RT 11 30-N

  • Bone-screw internal spinal fixation system, non-sterile
Titanium pre-bent longitudinal rod
SpineArt SA
MIS-RT 11 30-S
In Commercial Distribution

  • 07640178981881 ()

  • Outer Diameter: 5.4 Millimeter
  • Length: 130 Millimeter
MIS-RT 11 30-S

  • Bone-screw internal spinal fixation system, sterile
ROD TRIAL LONG
SpineArt SA
ELL-IN 24 02-N
In Commercial Distribution

  • 07640178981829 ()
ELL-IN 24 02-N

  • Spinal implant trial
ROD TRIAL SHORT
SpineArt SA
ELL-IN 24 01-N
In Commercial Distribution

  • 07640178981812 ()
ELL-IN 24 01-N

  • Spinal implant trial
SCREWDRIVER SHAFT PS
SpineArt SA
ELL-IN 05 03-N
In Commercial Distribution

  • 07640178981799 ()
ELL-IN 05 03-N

  • Surgical screwdriver, reusable
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