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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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No Description
SURETEK MEDICAL
6725-127-105
In Commercial Distribution

  • B39067251271051 ()


  • Surgical power tool system handpiece, sawing, line-powered
No Description
SURETEK MEDICAL
6125-127-100
In Commercial Distribution

  • B39061251271001 ()


  • Surgical power tool system handpiece, sawing, line-powered
No Description
SURETEK MEDICAL
6125-119-90
In Commercial Distribution

  • B3906125119901 ()


  • Surgical power tool system handpiece, sawing, line-powered
No Description
SURETEK MEDICAL
6118-89-75
In Commercial Distribution

  • B390611889751 ()


  • Surgical power tool system handpiece, sawing, line-powered
No Description
SURETEK MEDICAL
6118-119-90
In Commercial Distribution

  • B3906118119901 ()


  • Surgical power tool system handpiece, sawing, line-powered
CANNULA 96014 FEM 14ART 17VEN EA 17L
MEDTRONIC, INC.
96014
Not in Commercial Distribution

  • 00613994557100 ()

  • 14 FR Arterial
  • 17 FR Venous


  • Cardiopulmonary bypass cannula, femoral
CANNULA 96017 FEM 17ART 21VEN EA 17L
MEDTRONIC, INC.
96017
Not in Commercial Distribution

  • 00613994556752 ()

  • 21 FR Venous
  • 17 FR Arterial


  • Cardiopulmonary bypass cannula, femoral
CANNULA 96021 FEM 21ART 21VEN EA 17L
MEDTRONIC, INC.
96021
Not in Commercial Distribution

  • 00613994556745 ()

  • 21 FR Arterial
  • 21 FR Venous


  • Cardiopulmonary bypass cannula, femoral
CANNULA 96117 FEM 17ART 21VEN EA 17L
MEDTRONIC, INC.
96117
Not in Commercial Distribution

  • 00613994556738 ()

  • 17 FR Arterial
  • 21 FR Venous


  • Cardiopulmonary bypass cannula, femoral
CANNULA 96121 FEM 21ART 21VEN EA 17L
MEDTRONIC, INC.
96121
Not in Commercial Distribution

  • 00613994556721 ()

  • 21 FR Arterial
  • 21 FR Venous


  • Cardiopulmonary bypass cannula, femoral
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