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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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FOREFOOT FUSION REAMER CADDY
ARTHREX, INC.
AR-8944C-RC
In Commercial Distribution

  • 00888867052956 ()
AR-8944C-RC

  • Device sterilization/disinfection container, reusable
FOREFOOT FUSION MODULE INSTRUMENT CASE
ARTHREX, INC.
AR-8944C
In Commercial Distribution

  • 00888867052857 ()
AR-8944C

  • Device sterilization/disinfection container, reusable
ANKLE FRACTURE SYSTEM SCREW CADDY
ARTHREX, INC.
AR-8943C-SC
In Commercial Distribution

  • 00888867052697 ()
AR-8943C-SC

  • Device sterilization/disinfection container, reusable
ANKLE FRACTURE/DISTAL TIBIA SCREW CASE
ARTHREX, INC.
AR-8943C-31
In Commercial Distribution

  • 00888867052673 ()
AR-8943C-31

  • Device sterilization/disinfection container, reusable
ATTACHMENT SCREW, AIMING GUIDE
ARTHREX, INC.
AR-8943-37
In Commercial Distribution

  • 00888867052444 ()
AR-8943-37

  • Orthopaedic bone pin, non-bioabsorbable
AIMING GUIDE, FIBULA AVULSION PLATE
ARTHREX, INC.
AR-8943-35
In Commercial Distribution

  • 00888867052420 ()
AR-8943-35

  • Surgical drill guide, reusable
AIM GD LT,LOCK DISTAL FIBULA PLT
ARTHREX, INC.
AR-8943-34
In Commercial Distribution

  • 00888867052413 ()
AR-8943-34

  • Surgical drill guide, reusable
AIM GD RT,LOCK DISTAL FIBULA PLT
ARTHREX, INC.
AR-8943-33
In Commercial Distribution

  • 00888867052406 ()
AR-8943-33

  • Surgical drill guide, reusable
DRL SLVE,2.0MM FOR 2.7MM LOCK HOLE
ARTHREX, INC.
AR-8943-32
In Commercial Distribution

  • 00888867052390 ()
AR-8943-32

  • Orthopaedic implantation sleeve, reusable
DRILL GUIDE, 3.0 / 2.0MM
ARTHREX, INC.
AR-8943-31
In Commercial Distribution

  • 00888867052383 ()
AR-8943-31

  • Surgical drill guide, reusable
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