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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IQ COLUMBUS TRAY TRIAL FEM.COMP.STANDARD
Aesculap AG
NQ1014R
In Commercial Distribution

  • 04046964218408 ()
NQ1014R

  • Surgical instrument/implant rack
IQ COLUMBUS TRAY FEMUR PREPARATION
Aesculap AG
NQ1013R
In Commercial Distribution

  • 04046964217791 ()
NQ1013R

  • Surgical instrument/implant rack
IQ COLUMBUS/VEGA PS TRAY MANUAL INSTR.
Aesculap AG
NQ1012R
In Commercial Distribution

  • 04046964217784 ()
NQ1012R

  • Surgical instrument/implant rack
IQ COLUMBUS/VEGA PS TRAY GENERAL INSTR.
Aesculap AG
NQ1011R
In Commercial Distribution

  • 04046964217760 ()
NQ1011R

  • Surgical instrument/implant rack
QUINTEX DYNAMIC SCREW CADDY BASE
Aesculap AG
ME545P
In Commercial Distribution

  • 04046964203107 ()
ME545P

  • Surgical instrument/implant rack
QUINTEX CONSTRAINED SCREW CADDY BASE
Aesculap AG
ME544P
In Commercial Distribution

  • 04046964203091 ()
ME544P

  • Surgical instrument/implant rack
QUINTEX SEMICONSTRAINED SCREW CADDY BASE
Aesculap AG
ME543P
In Commercial Distribution

  • 04046964203084 ()
ME543P

  • Surgical instrument/implant rack
QUINTEX HYBRID PLATE CADDY BASE 5-LEVEL
Aesculap AG
ME542P
In Commercial Distribution

  • 04046964203077 ()
ME542P

  • Surgical instrument/implant rack
QUINTEX HYBRID PLATE CADDY BASE 4-LEVEL
Aesculap AG
ME541P
In Commercial Distribution

  • 04046964203060 ()
ME541P

  • Surgical instrument/implant rack
QUINTEX HYBRID PLATE CADDY BASE 3-LEVEL
Aesculap AG
ME540P
In Commercial Distribution

  • 04046964203053 ()
ME540P

  • Surgical instrument/implant rack
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