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.
E351410L
In Commercial Distribution

  • M684E351410L1 ()
  • 00192629248953 ()
E351410L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351324R
In Commercial Distribution

  • M684E351324R1 ()
  • 00192629248946 ()
E351324R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351324L
In Commercial Distribution

  • M684E351324L1 ()
  • 00192629248939 ()
E351324L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351322R
In Commercial Distribution

  • M684E351322R1 ()
  • 00192629248922 ()
E351322R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351320L
In Commercial Distribution

  • M684E351320L1 ()
  • 00192629248892 ()
E351320L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351317L
In Commercial Distribution

  • M684E351317L1 ()
  • 00192629248878 ()
E351317L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351314L
In Commercial Distribution

  • M684E351314L1 ()
  • 00192629248854 ()
E351314L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E63148RR
In Commercial Distribution

  • M684E63148RR1 ()
  • 00192629247901 ()
E63148RR

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E63147RR
In Commercial Distribution

  • M684E63147RR1 ()
  • 00192629247888 ()
E63147RR

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E63147RL
In Commercial Distribution

  • M684E63147RL1 ()
  • 00192629247871 ()
E63147RL

  • Knee revision prosthesis trial
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