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
SIGNATURE ORTHOPAEDICS PTY LTD
121-21-1202
In Commercial Distribution

  • 09348215077181 ()


  • Unicondylar knee prosthesis
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
121-21-1201
In Commercial Distribution

  • 09348215077174 ()


  • Unicondylar knee prosthesis
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
121-21-1102
In Commercial Distribution

  • 09348215077167 ()


  • Unicondylar knee prosthesis
No Description
SIGNATURE ORTHOPAEDICS PTY LTD
121-21-1101
In Commercial Distribution

  • 09348215077150 ()


  • Unicondylar knee prosthesis
IBAL UKA FEM CEMENTED SIZ 6,R-MEDIAL
ARTHREX, INC.
AR-501-UFRF
In Commercial Distribution

  • 00888867034358 ()
  • M150AR501UFRF2 ()
AR-501-UFRF

  • Unicondylar knee prosthesis
IBAL UKA FEM CEMENTED SIZ 5,R-MEDIAL
ARTHREX, INC.
AR-501-UFRE
In Commercial Distribution

  • 00888867034341 ()
  • M150AR501UFRE2 ()
AR-501-UFRE

  • Unicondylar knee prosthesis
IBAL UKA FEM CEMENTED SIZ 4,R-MEDIAL
ARTHREX, INC.
AR-501-UFRD
In Commercial Distribution

  • 00888867034334 ()
  • M150AR501UFRD2 ()
AR-501-UFRD

  • Unicondylar knee prosthesis
IBAL UKA FEM CEMENTED SIZ 3,R-MEDIAL
ARTHREX, INC.
AR-501-UFRC
In Commercial Distribution

  • 00888867034327 ()
  • M150AR501UFRC2 ()
AR-501-UFRC

  • Unicondylar knee prosthesis
IBAL UKA FEM CEMENTED SIZ 2,R-MEDIAL
ARTHREX, INC.
AR-501-UFRB
In Commercial Distribution

  • 00888867034310 ()
  • M150AR501UFRB2 ()
AR-501-UFRB

  • Unicondylar knee prosthesis
IBAL UKA FEM CEMENTED SIZ 1,R-MEDIAL
ARTHREX, INC.
AR-501-UFRA
In Commercial Distribution

  • 00888867034303 ()
  • M150AR501UFRA2 ()
AR-501-UFRA

  • Unicondylar knee prosthesis
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