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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COL REV F TRAY TRIAL STEMS/ST.PRP.C'LESS
Aesculap AG
NQ646R
In Commercial Distribution

  • 04046963403041 ()
NQ646R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY TIBIAL INSTR.SIZE 0
Aesculap AG
NQ632R
In Commercial Distribution

  • 04046963403034 ()
NQ632R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY PATELLA PREPARATION
Aesculap AG
NQ631R
In Commercial Distribution

  • 04046963403027 ()
NQ631R

  • Surgical instrument/implant rack
COL REV F TRAY REAMERS F/STEM PRP.C'LESS
Aesculap AG
NQ630R
In Commercial Distribution

  • 04046963403010 ()
NQ630R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY STEM PREP.CEMENTED
Aesculap AG
NQ629R
In Commercial Distribution

  • 04046963403003 ()
NQ629R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY TRIAL TIBIA SPACER
Aesculap AG
NQ628R
In Commercial Distribution

  • 04046963402976 ()
NQ628R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY TRIAL FEMORAL COMP.R
Aesculap AG
NQ627R
In Commercial Distribution

  • 04046963402969 ()
NQ627R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY TRIAL FEMORAL COMP.L
Aesculap AG
NQ626R
In Commercial Distribution

  • 04046963402952 ()
NQ626R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY TRIAL TIBIAL COMP.
Aesculap AG
NQ625R
In Commercial Distribution

  • 04046963402945 ()
NQ625R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY FEMORAL PREPARATION
Aesculap AG
NQ624R
In Commercial Distribution

  • 04046963402938 ()
NQ624R

  • Surgical instrument/implant rack
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