SEARCH RESULTS FOR: (*One Satoshitg:(@hkotccc)tFIg*)(280078 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.
E351620R
In Commercial Distribution

  • M684E351620R1 ()
  • 00192629249325 ()
E351620R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351620L
In Commercial Distribution

  • M684E351620L1 ()
  • 00192629249318 ()
E351620L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351617R
In Commercial Distribution

  • M684E351617R1 ()
  • 00192629249301 ()
E351617R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351617L
In Commercial Distribution

  • M684E351617L1 ()
  • 00192629249295 ()
E351617L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351614R
In Commercial Distribution

  • M684E351614R1 ()
  • 00192629249288 ()
E351614R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351614L
In Commercial Distribution

  • M684E351614L1 ()
  • 00192629249271 ()
E351614L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351612R
In Commercial Distribution

  • M684E351612R1 ()
  • 00192629249264 ()
E351612R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351612L
In Commercial Distribution

  • M684E351612L1 ()
  • 00192629249257 ()
E351612L

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351610R
In Commercial Distribution

  • M684E351610R1 ()
  • 00192629249240 ()
E351610R

  • Knee revision prosthesis trial
No Description
Microport Orthopedics Inc.
E351610L
In Commercial Distribution

  • M684E351610L1 ()
  • 00192629249233 ()
E351610L

  • Knee revision prosthesis trial
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