SEARCH RESULTS FOR: 得克萨斯A(1800206 results)

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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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RETRACTOR X0516119 DUAL BRK TBL 19MMX9CM
MEDTRONIC SOFAMOR DANEK, INC.
X0516119
In Commercial Distribution

  • 00643169789432 ()


  • General internal orthopaedic fixation system implantation kit
RETRACTOR X0516118 DUAL BRK TBL 19MMX8CM
MEDTRONIC SOFAMOR DANEK, INC.
X0516118
In Commercial Distribution

  • 00643169789425 ()


  • General internal orthopaedic fixation system implantation kit
DRIVER X1215009 TAMPONADE
MEDTRONIC SOFAMOR DANEK, INC.
X1215009
In Commercial Distribution

  • 00643169789326 ()


  • Surgical screwdriver, reusable
TAMPONADE X0116067 4.5 X 50
MEDTRONIC SOFAMOR DANEK, INC.
X0116067
In Commercial Distribution

  • 00643169789319 ()


  • Bone tap, reusable
TAMPONADE X0116065 4.5 X 40
MEDTRONIC SOFAMOR DANEK, INC.
X0116065
In Commercial Distribution

  • 00643169789296 ()


  • Bone tap, reusable
CURETTE X0516125 BAYONT LFT RVERSE 5.2MM
MEDTRONIC SOFAMOR DANEK, INC.
X0516125
Not in Commercial Distribution

  • 00643169788824 ()


  • Neurosurgical curette, single-use
CURETTE X0516124 BAYONT RHT RVERSE 5.2MM
MEDTRONIC SOFAMOR DANEK, INC.
X0516124
Not in Commercial Distribution

  • 00643169788817 ()


  • Neurosurgical curette, single-use
CURETTE X0516123 BAYONT LFT RVERSE 3.6MM
MEDTRONIC SOFAMOR DANEK, INC.
X0516123
Not in Commercial Distribution

  • 00643169788800 ()


  • Neurosurgical curette, single-use
CURETTE X0516122 BAYONT RHT RVERSE 3.6MM
MEDTRONIC SOFAMOR DANEK, INC.
X0516122
Not in Commercial Distribution

  • 00643169788794 ()


  • Neurosurgical curette, single-use
CURETTE X0516068 BAYONT LFT RVERSE 1.8MM
MEDTRONIC SOFAMOR DANEK, INC.
X0516068
In Commercial Distribution

  • 00643169788787 ()


  • Neurosurgical curette, single-use
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