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

Show Filters

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
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
< 1 ... 341 342 343 344 345 ... 409 >