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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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UNIVERS REVERS GLENOID PREP REAMER, LG
ARTHREX, INC.
AR-9128RF-03
In Commercial Distribution

  • 00888867193741 ()
AR-9128RF-03

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVERS GLENOID PREP REAMER, MED
ARTHREX, INC.
AR-9128RF-02
In Commercial Distribution

  • 00888867193734 ()
AR-9128RF-02

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVERS GLENOID PREP REAMER, SM
ARTHREX, INC.
AR-9128RF-01
In Commercial Distribution

  • 00888867193727 ()
AR-9128RF-01

  • Bone-resection orthopaedic reamer, reusable
2.8MM CANNULATED DRILL GUIDE, LARGE
ARTHREX, INC.
AR-9215-6CG
In Commercial Distribution

  • 00888867192614 ()
AR-9215-6CG

  • Surgical drill guide, reusable
2.8MM CANNULATED DRILL GUIDE, MEDIUM
ARTHREX, INC.
AR-9215-4CG
In Commercial Distribution

  • 00888867192607 ()
AR-9215-4CG

  • Surgical drill guide, reusable
2.8MM CANNULATED DRILL GUIDE, SMALL
ARTHREX, INC.
AR-9215-2CG
In Commercial Distribution

  • 00888867192591 ()
AR-9215-2CG

  • Surgical drill guide, reusable
Punch with cortical tap
ARTHREX, INC.
AR-1927PTB-45-2
In Commercial Distribution

  • 00888867190979 ()
AR-1927PTB-45-2

  • Orthopaedic implant impactor, reusable
Uni Revers Superolateral Version Adapter
ARTHREX, INC.
AR-9507RGSL-2
In Commercial Distribution

  • 00888867185937 ()
AR-9507RGSL-2

  • Surgical depth gauge, reusable
Uni Rev Superolateral Res Guide 135/155
ARTHREX, INC.
AR-9507RGSL-1
In Commercial Distribution

  • 00888867185920 ()
AR-9507RGSL-1

  • Surgical depth gauge, reusable
LAPIDUS SYSTEM ADDITIONAL PLATE CADDY
ARTHREX, INC.
AR-8941LS-APC
In Commercial Distribution

  • 00888867184800 ()
AR-8941LS-APC

  • Device sterilization/disinfection container, reusable
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