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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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BLADE 9563184 MIDLINE RIGHT 4
MEDTRONIC SOFAMOR DANEK, INC.
9563184
In Commercial Distribution

  • 00643169044036 ()


  • Surgical retraction system, reusable
BLADE 9563185 MIDLINE RIGHT 5
MEDTRONIC SOFAMOR DANEK, INC.
9563185
In Commercial Distribution

  • 00643169044029 ()


  • Surgical retraction system, reusable
BLADE 9563186 MIDLINE RIGHT 6
MEDTRONIC SOFAMOR DANEK, INC.
9563186
In Commercial Distribution

  • 00643169044012 ()


  • Surgical retraction system, reusable
BLADE 9563187 MIDLINE RIGHT 7
MEDTRONIC SOFAMOR DANEK, INC.
9563187
In Commercial Distribution

  • 00643169044005 ()


  • Surgical retraction system, reusable
BLADE 9563188 MIDLINE RIGHT 8
MEDTRONIC SOFAMOR DANEK, INC.
9563188
In Commercial Distribution

  • 00643169043992 ()


  • Surgical retraction system, reusable
BLADE 9563189 MIDLINE RIGHT 9
MEDTRONIC SOFAMOR DANEK, INC.
9563189
In Commercial Distribution

  • 00643169043985 ()


  • Surgical retraction system, reusable
BLADE 9563190 MIDLINE RIGHT 10
MEDTRONIC SOFAMOR DANEK, INC.
9563190
In Commercial Distribution

  • 00643169043978 ()


  • Surgical retraction system, reusable
BLADE 9563191 MIDLINE RIGHT 11
MEDTRONIC SOFAMOR DANEK, INC.
9563191
In Commercial Distribution

  • 00643169043961 ()


  • Surgical retraction system, reusable
TRAY 9563215 CORE MIDLINE
MEDTRONIC SOFAMOR DANEK, INC.
9563215
In Commercial Distribution

  • 00643169043824 ()


  • Instrument tray, reusable
DRIVER 5584305 CDHS 5.5/6.0 RMAS
MEDTRONIC SOFAMOR DANEK, INC.
5584305
In Commercial Distribution

  • 00643169043688 ()


  • Orthopaedic implant driver
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