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.
E351714L
In Commercial Distribution

  • M684E351714L1 ()
  • 00192629249554 ()
E351714L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351712R
In Commercial Distribution

  • M684E351712R1 ()
  • 00192629249547 ()
E351712R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351712L
In Commercial Distribution

  • M684E351712L1 ()
  • 00192629249530 ()
E351712L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351710R
In Commercial Distribution

  • M684E351710R1 ()
  • 00192629249523 ()
E351710R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351710L
In Commercial Distribution

  • M684E351710L1 ()
  • 00192629249516 ()
E351710L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351664R
In Commercial Distribution

  • M684E351664R1 ()
  • 00192629249509 ()
E351664R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351664L
In Commercial Distribution

  • M684E351664L1 ()
  • 00192629249493 ()
E351664L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351662R
In Commercial Distribution

  • M684E351662R1 ()
  • 00192629249486 ()
E351662R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351662L
In Commercial Distribution

  • M684E351662L1 ()
  • 00192629249479 ()
E351662L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351660R
In Commercial Distribution

  • M684E351660R1 ()
  • 00192629249462 ()
E351660R

  • Knee revision prosthesis trial
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