SEARCH RESULTS FOR: 得克萨斯A(1801707 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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RASP EX07101302 MED 14MM 8 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101302
In Commercial Distribution

  • 00613994853653 ()


  • Bone file/rasp, manual, reusable
RASP EX07101303 MED 16MM 8 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101303
In Commercial Distribution

  • 00613994853646 ()


  • Bone file/rasp, manual, reusable
RASP EX07101304 MED 18MM 8 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101304
In Commercial Distribution

  • 00613994853639 ()


  • Bone file/rasp, manual, reusable
RASP EX07101305 MED 20MM 8 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101305
In Commercial Distribution

  • 00613994853622 ()


  • Bone file/rasp, manual, reusable
RASP EX07101306 MED 10MM 12 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101306
In Commercial Distribution

  • 00613994853615 ()


  • Bone file/rasp, manual, reusable
RASP EX07101307 MED 12MM 12 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101307
In Commercial Distribution

  • 00613994853608 ()


  • Bone file/rasp, manual, reusable
RASP EX07101308 MED 14MM 12 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101308
In Commercial Distribution

  • 00613994853592 ()


  • Bone file/rasp, manual, reusable
RASP EX07101309 MED 16MM 12 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101309
In Commercial Distribution

  • 00613994853585 ()


  • Bone file/rasp, manual, reusable
RASP EX07101310 MED 18MM 12 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101310
In Commercial Distribution

  • 00613994853578 ()


  • Bone file/rasp, manual, reusable
RASP EX07101311 MED 20MM 12 DEG
MEDTRONIC SOFAMOR DANEK, INC.
EX07101311
In Commercial Distribution

  • 00613994853561 ()


  • Bone file/rasp, manual, reusable
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