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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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DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-11S
In Commercial Distribution

  • 00888867004917 ()
AR-1204RD-11S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-10S
In Commercial Distribution

  • 00888867004900 ()
AR-1204RD-10S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-105S
In Commercial Distribution

  • 00888867004894 ()
AR-1204RD-105S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-09S
In Commercial Distribution

  • 00888867004887 ()
AR-1204RD-09S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-095S
In Commercial Distribution

  • 00888867004870 ()
AR-1204RD-095S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-08S
In Commercial Distribution

  • 00888867004863 ()
AR-1204RD-08S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-085S
In Commercial Distribution

  • 00888867004856 ()
AR-1204RD-085S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-07S
In Commercial Distribution

  • 00888867004849 ()
AR-1204RD-07S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-075S
In Commercial Distribution

  • 00888867004832 ()
AR-1204RD-075S

  • Bone-resection orthopaedic reamer, single-use
DUAL RETROCUTTER
ARTHREX, INC.
AR-1204RD-06S
In Commercial Distribution

  • 00888867004825 ()
AR-1204RD-06S

  • Bone-resection orthopaedic reamer, single-use
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