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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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LIF, RASP, CC OFFSET, 14MM
ALPHATEC SPINE, INC.
256-16-100-14
In Commercial Distribution

  • 00190376394374 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 12MM
ALPHATEC SPINE, INC.
256-16-100-12
In Commercial Distribution

  • 00190376394367 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 10MM
ALPHATEC SPINE, INC.
256-16-100-10
In Commercial Distribution

  • 00190376394350 ()


  • Bone file/rasp, manual, reusable
LIF, RASP, CC OFFSET, 24MM
ALPHATEC SPINE, INC.
256-16-100-24
In Commercial Distribution

  • 00190376393223 ()


  • Bone file/rasp, manual, reusable
HERO DBM+ PASTE, 8 CC
SPINAL ELEMENTS, INC.
01002-008
In Commercial Distribution

  • 00840606104135 ()


  • Bone matrix implant, human-derived
HERO DBM+ PASTE, 3 CC
SPINAL ELEMENTS, INC.
01002-003
In Commercial Distribution

  • 00840606104128 ()


  • Bone matrix implant, human-derived
HERO DBM+ PASTE, 1 CC
SPINAL ELEMENTS, INC.
01002-001
In Commercial Distribution

  • 00840606104111 ()


  • Bone matrix implant, human-derived
HERO DBM PUTTY, 10 CC
SPINAL ELEMENTS, INC.
01001-010
In Commercial Distribution

  • 00840606104104 ()


  • Bone matrix implant, human-derived
HERO DBM PUTTY, 5 CC
SPINAL ELEMENTS, INC.
01001-005
In Commercial Distribution

  • 00840606104098 ()


  • Bone matrix implant, human-derived
HERO DBM PUTTY, 2.5 CC
SPINAL ELEMENTS, INC.
01001-002
In Commercial Distribution

  • 00840606104081 ()


  • Bone matrix implant, human-derived
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