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.
E351422L
In Commercial Distribution

  • M684E351422L1 ()
  • 00192629249059 ()
E351422L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351420R
In Commercial Distribution

  • M684E351420R1 ()
  • 00192629249042 ()
E351420R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351420L
In Commercial Distribution

  • M684E351420L1 ()
  • 00192629249035 ()
E351420L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351417R
In Commercial Distribution

  • M684E351417R1 ()
  • 00192629249028 ()
E351417R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351417L
In Commercial Distribution

  • M684E351417L1 ()
  • 00192629249011 ()
E351417L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351414R
In Commercial Distribution

  • M684E351414R1 ()
  • 00192629249004 ()
E351414R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351414L
In Commercial Distribution

  • M684E351414L1 ()
  • 00192629248991 ()
E351414L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351412R
In Commercial Distribution

  • M684E351412R1 ()
  • 00192629248984 ()
E351412R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351412L
In Commercial Distribution

  • M684E351412L1 ()
  • 00192629248977 ()
E351412L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351410R
In Commercial Distribution

  • M684E351410R1 ()
  • 00192629248960 ()
E351410R

  • Knee revision prosthesis trial
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