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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ADAPTER 9563081 FOCUS MIDLINE
MEDTRONIC SOFAMOR DANEK, INC.
9563081
In Commercial Distribution

  • 00643169044159 ()


  • Surgical retraction system, reusable
SPECULUM 9563082 MIDLINE
MEDTRONIC SOFAMOR DANEK, INC.
9563082
In Commercial Distribution

  • 00643169044142 ()


  • Surgical retraction system, reusable
WEITLANER 9563083 MIDLINE
MEDTRONIC SOFAMOR DANEK, INC.
9563083
In Commercial Distribution

  • 00643169044135 ()


  • Surgical retraction system, reusable
BLADE 9563084 MIDLINE LEFT 4
MEDTRONIC SOFAMOR DANEK, INC.
9563084
In Commercial Distribution

  • 00643169044128 ()


  • Surgical retraction system, reusable
BLADE 9563085 MIDLINE LEFT 5
MEDTRONIC SOFAMOR DANEK, INC.
9563085
In Commercial Distribution

  • 00643169044111 ()


  • Surgical retraction system, reusable
BLADE 9563086 MIDLINE LEFT 6
MEDTRONIC SOFAMOR DANEK, INC.
9563086
In Commercial Distribution

  • 00643169044104 ()


  • Surgical retraction system, reusable
BLADE 9563087 MIDLINE LEFT 7
MEDTRONIC SOFAMOR DANEK, INC.
9563087
In Commercial Distribution

  • 00643169044098 ()


  • Surgical retraction system, reusable
BLADE 9563088 MIDLINE LEFT 8
MEDTRONIC SOFAMOR DANEK, INC.
9563088
In Commercial Distribution

  • 00643169044081 ()


  • Surgical retraction system, reusable
BLADE 9563089 MIDLINE LEFT 9
MEDTRONIC SOFAMOR DANEK, INC.
9563089
In Commercial Distribution

  • 00643169044074 ()


  • Surgical retraction system, reusable
BLADE 9563090 MIDLINE LEFT 10
MEDTRONIC SOFAMOR DANEK, INC.
9563090
In Commercial Distribution

  • 00643169044067 ()


  • Surgical retraction system, reusable
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