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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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Right Facing Serrated Curette Bayoneted, Size #3
K2M, INC.
AG01-92012
In Commercial Distribution

  • 10888857423077 ()
AG01-92012

  • Bone curette, reusable
Right Angled Convex Rasp Bayoneted,
K2M, INC.
AG01-92011
In Commercial Distribution

  • 10888857423060 ()
AG01-92011

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Left Angled Convex Rasp Bayoneted,
K2M, INC.
AG01-92010
In Commercial Distribution

  • 10888857423053 ()
AG01-92010

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Convex Rasp Bayoneted
K2M, INC.
AG01-92009
In Commercial Distribution

  • 10888857423046 ()
AG01-92009

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Angled Pusher Bayoneted
K2M, INC.
AG01-92018
In Commercial Distribution

  • 10888857423039 ()
AG01-92018

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Pusher Bayoneted
K2M, INC.
AG01-92017
In Commercial Distribution

  • 10888857423022 ()
AG01-92017

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Right Angled Pull Stirrup Curette Bayoneted,
K2M, INC.
AG01-92008
In Commercial Distribution

  • 10888857423015 ()
AG01-92008

  • Bone curette, reusable
Left Angled Pull Stirrup Curette Bayoneted,
K2M, INC.
AG01-92007
In Commercial Distribution

  • 10888857423008 ()
AG01-92007

  • Bone curette, reusable
Left Facing Pull Stirrup Curette Bayoneted,
K2M, INC.
AG01-92006
In Commercial Distribution

  • 10888857422995 ()
AG01-92006

  • Bone curette, reusable
Right Facing Pull Stirrup Curette Bayoneted,
K2M, INC.
AG01-92005
In Commercial Distribution

  • 10888857422988 ()
AG01-92005

  • Bone curette, reusable
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