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.
E351822L
In Commercial Distribution

  • M684E351822L1 ()
  • 00192629249752 ()
E351822L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351820R
In Commercial Distribution

  • M684E351820R1 ()
  • 00192629249745 ()
E351820R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351820L
In Commercial Distribution

  • M684E351820L1 ()
  • 00192629249738 ()
E351820L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351817R
In Commercial Distribution

  • M684E351817R1 ()
  • 00192629249721 ()
E351817R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351817L
In Commercial Distribution

  • M684E351817L1 ()
  • 00192629249714 ()
E351817L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351814R
In Commercial Distribution

  • M684E351814R1 ()
  • 00192629249707 ()
E351814R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351814L
In Commercial Distribution

  • M684E351814L1 ()
  • 00192629249691 ()
E351814L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351812R
In Commercial Distribution

  • M684E351812R1 ()
  • 00192629249684 ()
E351812R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351812L
In Commercial Distribution

  • M684E351812L1 ()
  • 00192629249677 ()
E351812L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351810R
In Commercial Distribution

  • M684E351810R1 ()
  • 00192629249660 ()
E351810R

  • Knee revision prosthesis trial
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