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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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Rasp Trial Head, 38X28 Lordotic 8°, 17L
SPINEFRONTIER, INC.
11-81042-17
In Commercial Distribution

  • 00190361038979 ()


  • Polymeric spinal interbody fusion cage
Rasp Trial Head, 38X28 Lordotic 8°, 15L
SPINEFRONTIER, INC.
11-81042-15
In Commercial Distribution

  • 00190361038962 ()


  • Polymeric spinal interbody fusion cage
Rasp Trial Head, 38X28 Lordotic 8°, 13L
SPINEFRONTIER, INC.
11-81042-13
In Commercial Distribution

  • 00190361038955 ()


  • Polymeric spinal interbody fusion cage
Rasp Trial Head, 38X28 Lordotic 8°, 9L
SPINEFRONTIER, INC.
11-81042-09
In Commercial Distribution

  • 00190361038931 ()


  • Polymeric spinal interbody fusion cage
Flat Trial Head, 38X28 Lordotic 8°, 19L
SPINEFRONTIER, INC.
11-81023-19
In Commercial Distribution

  • 00190361038924 ()


  • Polymeric spinal interbody fusion cage
Flat Trial Head, 38X28 Lordotic 8°, 17L
SPINEFRONTIER, INC.
11-81023-17
In Commercial Distribution

  • 00190361038917 ()


  • Polymeric spinal interbody fusion cage
Flat Trial Head, 38X28 Lordotic 8°, 13L
SPINEFRONTIER, INC.
11-81023-13
In Commercial Distribution

  • 00190361038894 ()


  • Polymeric spinal interbody fusion cage
Flat Trial Head, 38X28 Lordotic 8°, 9L
SPINEFRONTIER, INC.
11-81023-09
In Commercial Distribution

  • 00190361038870 ()


  • Polymeric spinal interbody fusion cage
Rasp Trial Head, 35X26 Lordotic 8° 15L
SPINEFRONTIER, INC.
11-81028-15
In Commercial Distribution

  • 00190361038856 ()


  • Polymeric spinal interbody fusion cage
TRIAL RASP, LORDOTIC, 19MM WIDE, 8MM
SPINEFRONTIER, INC.
11-50119-08
In Commercial Distribution

  • 00190361038436 ()


  • Polymeric spinal interbody fusion cage
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