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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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ACF TRIAL SPACER RASP-PARALLEL 7MM HEIGHT
Synthes GmbH
03.810.013
In Commercial Distribution

  • H981038100130 ()
  • 10705034727158 ()
03810013

  • Bone file/rasp, manual, reusable
ACF TRIAL SPACER RASP-PARALLEL 5MM HEIGHT
Synthes GmbH
03.810.011
In Commercial Distribution

  • H981038100110 ()
  • 10705034727134 ()
03810011

  • Bone file/rasp, manual, reusable
ACF TRIAL SPACER RASP-LORDOTIC 11MM HEIGHT
Synthes GmbH
03.810.007
In Commercial Distribution

  • H981038100070 ()
  • 10705034727110 ()
03810007

  • Bone file/rasp, manual, reusable
ACF TRIAL SPACER RASP-LORDOTIC 9MM HEIGHT
Synthes GmbH
03.810.005
In Commercial Distribution

  • H981038100050 ()
  • 10705034727097 ()
03810005

  • Bone file/rasp, manual, reusable
ACF TRIAL SPACER RASP-LORDOTIC 7MM HEIGHT
Synthes GmbH
03.810.003
In Commercial Distribution

  • H981038100030 ()
  • 10705034727073 ()
03810003

  • Bone file/rasp, manual, reusable
ACF TRIAL SPACER RASP-LORDOTIC 6MM HEIGHT
Synthes GmbH
03.810.002
In Commercial Distribution

  • H981038100020 ()
  • 10705034727066 ()
03810002

  • Bone file/rasp, manual, reusable
SPREADER 11MM HEIGHT
Synthes GmbH
03.809.876
In Commercial Distribution

  • 07611819325821 ()
  • H981038098760 ()
  • 10705034726441 ()
03809876

  • Bone distraction forceps
ORACLE RASP
Synthes GmbH
03.809.849
In Commercial Distribution

  • 07611819325616 ()
  • H981038098490 ()
  • 10705034726229 ()
03809849

  • Bone file/rasp, manual, reusable
SPREADER-ANGLED 6MM HEIGHT
Synthes GmbH
03.809.777
In Commercial Distribution

  • H981038097770 ()
  • 10705034725994 ()
03809777

  • Bone distraction forceps
RASP-ANGLED RIGHT
Synthes GmbH
03.809.770
In Commercial Distribution

  • H981038097700 ()
  • 10705034725925 ()
03809770

  • Bone file/rasp, manual, reusable
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