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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QUINTEX HYBRID PLATE CADDY BASE 2-LEVEL
Aesculap AG
ME539P
In Commercial Distribution

  • 04046964203046 ()
ME539P

  • Surgical instrument/implant rack
QUINTEX HYBRID PLATE CADDY BASE 1-LEVEL
Aesculap AG
ME538P
In Commercial Distribution

  • 04046964203039 ()
ME538P

  • Surgical instrument/implant rack
QUINTEX DYNAMIC PLATE CADDY BASE 5-LEVEL
Aesculap AG
ME534P
In Commercial Distribution

  • 04046964202988 ()
ME534P

  • Surgical instrument/implant rack
QUINTEX DYNAMIC PLATE CADDY BASE 4-LEVEL
Aesculap AG
ME533P
In Commercial Distribution

  • 04046964202971 ()
ME533P

  • Surgical instrument/implant rack
QUINTEX DYNAMIC PLATE CADDY BASE 3-LEVEL
Aesculap AG
ME532P
In Commercial Distribution

  • 04046964202957 ()
ME532P

  • Surgical instrument/implant rack
QUINTEX DYNAMIC PLATE CADDY BASE 2-LEVEL
Aesculap AG
ME531P
In Commercial Distribution

  • 04046964202940 ()
ME531P

  • Surgical instrument/implant rack
QUINTEX DYNAMIC PLATE CADDY BASE 1-LEVEL
Aesculap AG
ME530P
In Commercial Distribution

  • 04046964202926 ()
ME530P

  • Surgical instrument/implant rack
QUINTEX HYBRID PLATE CADDY LID 5-LEVEL
Aesculap AG
ME267P
In Commercial Distribution

  • 04046964202919 ()
ME267P

  • Surgical instrument/implant rack
QUINTEX HYBRID PLATE CADDY LID 4-LEVEL
Aesculap AG
ME266P
In Commercial Distribution

  • 04046964202896 ()
ME266P

  • Surgical instrument/implant rack
QUINTEX HYBRID PLATE CADDY LID 3-LEVEL
Aesculap AG
ME265P
In Commercial Distribution

  • 04046964202889 ()
ME265P

  • Surgical instrument/implant rack
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