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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 Class Implantable

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ALIF SPREADER-SHORT 10MM HEIGHT
Synthes GmbH
SD03.808.010
In Commercial Distribution

  • H981SD038080100 ()
  • 10705034704265 ()
SD03808010

  • Bone distraction forceps
ALIF SPREADER-SHORT 9MM HEIGHT
Synthes GmbH
SD03.808.009
In Commercial Distribution

  • H981SD038080090 ()
  • 10705034704258 ()
SD03808009

  • Bone distraction forceps
ALIF SPREADER-SHORT 8MM HEIGHT
Synthes GmbH
SD03.808.008
In Commercial Distribution

  • H981SD038080080 ()
  • 10705034704241 ()
SD03808008

  • Bone distraction forceps
ALIF SPREADER-SHORT 7MM HEIGHT
Synthes GmbH
SD03.808.007
In Commercial Distribution

  • H981SD038080070 ()
  • 10705034704234 ()
SD03808007

  • Bone distraction forceps
ALIF SPREADER HANDLE-LONG
Synthes GmbH
SD03.808.004
In Commercial Distribution

  • H981SD038080040 ()
  • 10705034704227 ()
SD03808004

  • Bone distraction forceps
TEMPORARY DISTRACTION PEG BAYONETED
Synthes GmbH
SD03.641.020
In Commercial Distribution

  • H981SD036410200 ()
  • 10705034703381 ()
SD03641020

  • Bone distraction forceps
CURVED RASP/SMALL-RIGHT
Synthes GmbH
SD389.836
In Commercial Distribution

  • H981SD3898360 ()
  • 10705034708324 ()
SD389836

  • Bone file/rasp, manual, reusable
CURVED RASP/SMALL-LEFT
Synthes GmbH
SD389.835
In Commercial Distribution

  • H981SD3898350 ()
  • 10705034708317 ()
SD389835

  • Bone file/rasp, manual, reusable
BONE RASP 11MM/2MM TEETH
Synthes GmbH
SD389.718
In Commercial Distribution

  • H981SD3897180 ()
  • 10705034708065 ()
SD389718

  • Bone file/rasp, manual, reusable
BONE RASP 9MM/2MM TEETH
Synthes GmbH
SD389.717
In Commercial Distribution

  • H981SD3897170 ()
  • 10705034708058 ()
SD389717

  • Bone file/rasp, manual, reusable
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