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 Type Device Class Implantable

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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
COLUMBUS REV F TRAY MANUAL TIBIA INSTR.
Aesculap AG
NQ623R
In Commercial Distribution

  • 04046963402921 ()
NQ623R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY MANUAL FEMUR INSTR.
Aesculap AG
NQ622R
In Commercial Distribution

  • 04046963402914 ()
NQ622R

  • Surgical instrument/implant rack
COLUMBUS REV F TRAY GENERAL INSTRUMENTS
Aesculap AG
NQ621R
In Commercial Distribution

  • 04046963402907 ()
NQ621R

  • Surgical instrument/implant rack
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