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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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AccelFix-XL, 9°, 45X22X10mm
L&K BIOMED CO. ,LTD.
L4522-1009S
In Commercial Distribution

  • 08800061635621 ()
L4522-1009S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 9°, 45X22X8mm
L&K BIOMED CO. ,LTD.
L4522-0809S
In Commercial Distribution

  • 08800061635614 ()
L4522-0809S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 6°, 45X22X12mm
L&K BIOMED CO. ,LTD.
L4522-1206S
In Commercial Distribution

  • 08800061635607 ()
L4522-1206S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 6°, 45X22X10mm
L&K BIOMED CO. ,LTD.
L4522-1006S
In Commercial Distribution

  • 08800061635591 ()
L4522-1006S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 6°, 45X22X8mm
L&K BIOMED CO. ,LTD.
L4522-0806S
In Commercial Distribution

  • 08800061635584 ()
L4522-0806S

  • Polymeric spinal interbody fusion cage
AccelFix-XL, 0°, 45X22X10mm
L&K BIOMED CO. ,LTD.
L4522-1000S
In Commercial Distribution

  • 08800061635560 ()
L4522-1000S

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

  • 08800061635522 ()
L4022-0812S

  • 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, 6°, 40X22X12mm
L&K BIOMED CO. ,LTD.
L4022-1206S
In Commercial Distribution

  • 08800061635485 ()
L4022-1206S

  • Polymeric spinal interbody fusion cage
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