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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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AccelFix-XL, 12°, 40X22X12mm
L&K BIOMED CO. ,LTD.
L4022-1212S
In Commercial Distribution

  • 08800061635546 ()
L4022-1212S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 12°, 40X22X10mm
L&K BIOMED CO. ,LTD.
L4022-1012S
In Commercial Distribution

  • 08800061635539 ()
L4022-1012S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 12°, 40X22X8mm
L&K BIOMED CO. ,LTD.
L4022-0812S
In Commercial Distribution

  • 08800061635522 ()
L4022-0812S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 9°, 40X22X12mm
L&K BIOMED CO. ,LTD.
L4022-1209S
In Commercial Distribution

  • 08800061635515 ()
L4022-1209S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 9°, 40X22X10mm
L&K BIOMED CO. ,LTD.
L4022-1009S
In Commercial Distribution

  • 08800061635508 ()
L4022-1009S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 9°, 40X22X8mm
L&K BIOMED CO. ,LTD.
L4022-0809S
In Commercial Distribution

  • 08800061635492 ()
L4022-0809S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 6°, 40X22X12mm
L&K BIOMED CO. ,LTD.
L4022-1206S
In Commercial Distribution

  • 08800061635485 ()
L4022-1206S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 6°, 40X22X10mm
L&K BIOMED CO. ,LTD.
L4022-1006S
In Commercial Distribution

  • 08800061635478 ()
L4022-1006S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 6°, 40X22X8mm
L&K BIOMED CO. ,LTD.
L4022-0806S
In Commercial Distribution

  • 08800061635461 ()
L4022-0806S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 0°, 40X22X12mm
L&K BIOMED CO. ,LTD.
L4022-1200S
In Commercial Distribution

  • 08800061635454 ()
L4022-1200S

  • Polymeric spinal interbody fusion cage
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