SEARCH RESULTS FOR: 得克萨斯A(22647 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.
E351314R
In Commercial Distribution

  • M684E351314R1 ()
  • 00192629248861 ()
E351314R

  • 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.
E351312R
In Commercial Distribution

  • M684E351312R1 ()
  • 00192629248847 ()
E351312R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351312L
In Commercial Distribution

  • M684E351312L1 ()
  • 00192629248830 ()
E351312L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351310R
In Commercial Distribution

  • M684E351310R1 ()
  • 00192629248823 ()
E351310R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351310L
In Commercial Distribution

  • M684E351310L1 ()
  • 00192629248816 ()
E351310L

  • 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.
E63148RL
In Commercial Distribution

  • M684E63148RL1 ()
  • 00192629247895 ()
E63148RL

  • 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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