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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-06S
In Commercial Distribution

  • 00888867004825 ()
AR-1204RD-06S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 12MM
ARTHREX, INC.
AR-1204R-12S
In Commercial Distribution

  • 00888867004801 ()
AR-1204R-12S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 11 MM
ARTHREX, INC.
AR-1204R-11S
In Commercial Distribution

  • 00888867004795 ()
AR-1204R-11S

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

  • 00888867004788 ()
AR-1204R-10S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 10.5 MM
ARTHREX, INC.
AR-1204R-105S
In Commercial Distribution

  • 00888867004771 ()
AR-1204R-105S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 9 MM
ARTHREX, INC.
AR-1204R-09S
In Commercial Distribution

  • 00888867004764 ()
AR-1204R-09S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 9.5 MM
ARTHREX, INC.
AR-1204R-095S
In Commercial Distribution

  • 00888867004757 ()
AR-1204R-095S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 8 MM
ARTHREX, INC.
AR-1204R-08S
In Commercial Distribution

  • 00888867004740 ()
AR-1204R-08S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 8.5 MM
ARTHREX, INC.
AR-1204R-085S
In Commercial Distribution

  • 00888867004733 ()
AR-1204R-085S

  • Bone-resection orthopaedic reamer, single-use
RETROCUTTER, 7 MM
ARTHREX, INC.
AR-1204R-07S
In Commercial Distribution

  • 00888867004726 ()
AR-1204R-07S

  • Bone-resection orthopaedic reamer, single-use
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