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.
E351810L
In Commercial Distribution

  • M684E351810L1 ()
  • 00192629249653 ()
E351810L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351724R
In Commercial Distribution

  • M684E351724R1 ()
  • 00192629249646 ()
E351724R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351724L
In Commercial Distribution

  • M684E351724L1 ()
  • 00192629249639 ()
E351724L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351722R
In Commercial Distribution

  • M684E351722R1 ()
  • 00192629249622 ()
E351722R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351722L
In Commercial Distribution

  • M684E351722L1 ()
  • 00192629249615 ()
E351722L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351720R
In Commercial Distribution

  • M684E351720R1 ()
  • 00192629249608 ()
E351720R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351720L
In Commercial Distribution

  • M684E351720L1 ()
  • 00192629249592 ()
E351720L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351717R
In Commercial Distribution

  • M684E351717R1 ()
  • 00192629249585 ()
E351717R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351717L
In Commercial Distribution

  • M684E351717L1 ()
  • 00192629249578 ()
E351717L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351714R
In Commercial Distribution

  • M684E351714R1 ()
  • 00192629249561 ()
E351714R

  • Knee revision prosthesis trial
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