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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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CUTTER X0599105 9CM-11CM DPTH X 5 DIA
MEDTRONIC SOFAMOR DANEK, INC.
X0599105
In Commercial Distribution

  • 00673978815862 ()


  • Orthopaedic knife
RING CURETTE,175 DEG, SIZE 6
MEDTRONIC SOFAMOR DANEK, INC.
X0599097
In Commercial Distribution

  • 00673978815848 ()


  • Bone curette, reusable
RING CURETTE,135 DEG, SIZE 6
MEDTRONIC SOFAMOR DANEK, INC.
X0599096
In Commercial Distribution

  • 00673978815831 ()


  • Bone curette, reusable
RING CURETTE, 90DEG, SIZE 6
MEDTRONIC SOFAMOR DANEK, INC.
X0599095
In Commercial Distribution

  • 00673978815824 ()


  • Bone curette, reusable
MOD.LATERAL IMPLANT HOLDER
MEDTRONIC SOFAMOR DANEK, INC.
X0599063
In Commercial Distribution

  • 00673978815534 ()


  • Surgical implant/trial-implant/sizer holder, reusable
TRIMLINE MOD BLADE 20 X 50MM
MEDTRONIC SOFAMOR DANEK, INC.
X0599061
In Commercial Distribution

  • 00673978815510 ()


  • Orthopaedic knife
TRIMLINE MOD BLADE 20 X 40MM
MEDTRONIC SOFAMOR DANEK, INC.
X0599060
In Commercial Distribution

  • 00673978815503 ()


  • Orthopaedic knife
WIRE X0599052 UCSS THREADED L 35
MEDTRONIC SOFAMOR DANEK, INC.
X0599052
In Commercial Distribution

  • 00673978815428 ()


  • Spinal guidewire
ATLANTIS VA GUIDE W/WINDOW
MEDTRONIC SOFAMOR DANEK, INC.
X0599050
In Commercial Distribution

  • 00673978815404 ()


  • General internal orthopaedic fixation system implantation kit
ATLANTIS FIXED GUIDE W/WINDOW
MEDTRONIC SOFAMOR DANEK, INC.
X0599049
In Commercial Distribution

  • 00673978815398 ()


  • General internal orthopaedic fixation system implantation kit
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