SEARCH RESULTS FOR: hibcc(4480 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 Class Implantable

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No Description
Microport Orthopedics Inc.
E351654L
In Commercial Distribution

  • M684E351654L1 ()
  • 00192629249417 ()
E351654L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351652R
In Commercial Distribution

  • M684E351652R1 ()
  • 00192629249400 ()
E351652R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351652L
In Commercial Distribution

  • M684E351652L1 ()
  • 00192629249394 ()
E351652L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351650R
In Commercial Distribution

  • M684E351650R1 ()
  • 00192629249387 ()
E351650R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351650L
In Commercial Distribution

  • M684E351650L1 ()
  • 00192629249370 ()
E351650L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351624R
In Commercial Distribution

  • M684E351624R1 ()
  • 00192629249363 ()
E351624R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351624L
In Commercial Distribution

  • M684E351624L1 ()
  • 00192629249356 ()
E351624L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351622R
In Commercial Distribution

  • M684E351622R1 ()
  • 00192629249349 ()
E351622R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351622L
In Commercial Distribution

  • M684E351622L1 ()
  • 00192629249332 ()
E351622L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351620R
In Commercial Distribution

  • M684E351620R1 ()
  • 00192629249325 ()
E351620R

  • Knee revision prosthesis trial
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