SEARCH RESULTS FOR: Femoral(4450 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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No Description
Microport Orthopedics Inc.
E351517L
In Commercial Distribution

  • M684E351517L1 ()
  • 00192629249158 ()
E351517L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351514R
In Commercial Distribution

  • M684E351514R1 ()
  • 00192629249141 ()
E351514R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351514L
In Commercial Distribution

  • M684E351514L1 ()
  • 00192629249134 ()
E351514L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351512R
In Commercial Distribution

  • M684E351512R1 ()
  • 00192629249127 ()
E351512R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351512L
In Commercial Distribution

  • M684E351512L1 ()
  • 00192629249110 ()
E351512L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351510R
In Commercial Distribution

  • M684E351510R1 ()
  • 00192629249103 ()
E351510R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351510L
In Commercial Distribution

  • M684E351510L1 ()
  • 00192629249097 ()
E351510L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351424R
In Commercial Distribution

  • M684E351424R1 ()
  • 00192629249080 ()
E351424R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351424L
In Commercial Distribution

  • M684E351424L1 ()
  • 00192629249073 ()
E351424L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351422R
In Commercial Distribution

  • M684E351422R1 ()
  • 00192629249066 ()
E351422R

  • Knee revision prosthesis trial
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