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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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LTX DOMED SPACER, 6 x 18 x 60 mm, 20°
ALPHATEC SPINE, INC.
261-06186020-D
In Commercial Distribution

  • 00190376522807 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 18 x 60 mm, 20°
ALPHATEC SPINE, INC.
261-06186020
In Commercial Distribution

  • 00190376522784 ()


  • Polymeric spinal interbody fusion cage
LTX DOMED SPACER, 6 x 18 x 60 mm, 15°
ALPHATEC SPINE, INC.
261-06186015-D
In Commercial Distribution

  • 00190376522777 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 18 x 60 mm, 15°
ALPHATEC SPINE, INC.
261-06186015
In Commercial Distribution

  • 00190376522760 ()


  • Polymeric spinal interbody fusion cage
LTX DOMED SPACER, 6 x 18 x 55 mm, 20°
ALPHATEC SPINE, INC.
261-06185520-D
In Commercial Distribution

  • 00190376522753 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 18 x 55 mm, 20°
ALPHATEC SPINE, INC.
261-06185520
In Commercial Distribution

  • 00190376522746 ()


  • Polymeric spinal interbody fusion cage
LTX DOMED SPACER, 6 x 18 x 55 mm, 15°
ALPHATEC SPINE, INC.
261-06185515-D
In Commercial Distribution

  • 00190376522739 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 18 x 55 mm, 15°
ALPHATEC SPINE, INC.
261-06185515
In Commercial Distribution

  • 00190376522722 ()


  • Polymeric spinal interbody fusion cage
LTX DOMED SPACER, 6 x 18 x 50 mm, 20°
ALPHATEC SPINE, INC.
261-06185020-D
In Commercial Distribution

  • 00190376522715 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 18 x 50 mm, 20°
ALPHATEC SPINE, INC.
261-06185020
In Commercial Distribution

  • 00190376522708 ()


  • Polymeric spinal interbody fusion cage
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