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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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SCRAPER EX1016023 STRAIGHT BOX 12MM
MEDTRONIC SOFAMOR DANEK, INC.
EX1016023
Not in Commercial Distribution

  • 00643169888722 ()


  • Bone curette, reusable
SCRAPER EX1016022 STRAIGHT BOX 10MM
MEDTRONIC SOFAMOR DANEK, INC.
EX1016022
Not in Commercial Distribution

  • 00643169888715 ()


  • Bone curette, reusable
SCRAPER EX1016021 STRAIGHT BOX 8MM
MEDTRONIC SOFAMOR DANEK, INC.
EX1016021
Not in Commercial Distribution

  • 00643169888708 ()


  • Bone curette, reusable
SCRAPER EX1016020 STRAIGHT BOX 6MM
MEDTRONIC SOFAMOR DANEK, INC.
EX1016020
Not in Commercial Distribution

  • 00643169888692 ()


  • Bone curette, reusable
BLADE EX0916065 MIDLIF 10CM-R
MEDTRONIC SOFAMOR DANEK, INC.
EX0916065
In Commercial Distribution

  • 00643169886711 ()


  • General internal orthopaedic fixation system implantation kit
BLADE EX0916064 MIDLIF 9CM-R
MEDTRONIC SOFAMOR DANEK, INC.
EX0916064
In Commercial Distribution

  • 00643169886704 ()


  • General internal orthopaedic fixation system implantation kit
BLADE EX0916063 MIDLIF 8CM-R
MEDTRONIC SOFAMOR DANEK, INC.
EX0916063
In Commercial Distribution

  • 00643169886698 ()


  • General internal orthopaedic fixation system implantation kit
BLADE EX0916062 MIDLIF 7CM-R
MEDTRONIC SOFAMOR DANEK, INC.
EX0916062
In Commercial Distribution

  • 00643169886681 ()


  • General internal orthopaedic fixation system implantation kit
BLADE EX0916061 MIDLIF 6CM-R
MEDTRONIC SOFAMOR DANEK, INC.
EX0916061
In Commercial Distribution

  • 00643169886674 ()


  • General internal orthopaedic fixation system implantation kit
BLADE EX0916060 MIDLIF 5CM-R
MEDTRONIC SOFAMOR DANEK, INC.
EX0916060
In Commercial Distribution

  • 00643169886667 ()


  • General internal orthopaedic fixation system implantation kit
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