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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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REFURB 11.0 DILATOR
Smith & Nephew, Inc.
7207649D
In Commercial Distribution

  • 00885556504659 ()
7207649D

  • Bone awl, reusable
FLUTED CURVED CANNULATED AWL
Smith & Nephew, Inc.
E0016568-1
In Commercial Distribution

  • 00885556756188 ()
E0016568-1

  • Bone awl, reusable
FLUTED CURVED CANNULATED AWL
Smith & Nephew, Inc.
E0016001-1
In Commercial Distribution

  • 00885556717332 ()
E0016001-1

  • Bone awl, reusable
FLUTED CURVED CANNULATED AWL
Smith & Nephew, Inc.
E0015998-1
In Commercial Distribution

  • 00885556717325 ()
E0015998-1

  • Bone awl, reusable
EXTENDED AWL
MEDTRONIC SOFAMOR DANEK, INC.
X8691000
In Commercial Distribution

  • 00721902059483 ()


  • Bone awl, reusable
INSTRUMENT 8646012 AWL PEDICULAR STAPLE
MEDTRONIC SOFAMOR DANEK, INC.
8646012
In Commercial Distribution

  • 00721902055232 ()


  • Bone awl, reusable
4.0 X 13MM AWL / TAP
MEDTRONIC SOFAMOR DANEK, INC.
X1001016
In Commercial Distribution

  • 00721902277061 ()


  • Bone awl, reusable
AWL / STAPLE DRIVER W/ EXT TIP
MEDTRONIC SOFAMOR DANEK, INC.
X0901030
In Commercial Distribution

  • 00721902213939 ()


  • Bone awl, reusable
SHORT SACRAL X1001015 AWL
MEDTRONIC SOFAMOR DANEK, INC.
X1001015
In Commercial Distribution

  • 00721902275838 ()


  • Bone awl, reusable
INSTRUMENT 8968004 RETRACTABLE AWL
MEDTRONIC SOFAMOR DANEK, INC.
8968004
In Commercial Distribution

  • 00721902230745 ()


  • Bone awl, reusable
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