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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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UNIVERS REVS STEM/CUP EXTRACT ADPTR HNDL
ARTHREX, INC.
AR-9512
In Commercial Distribution

  • 00888867061866 ()
AR-9512

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVS RMR GD-155 (+2MM R/H)
ARTHREX, INC.
AR-9511RG-R
In Commercial Distribution

  • 00888867061859 ()
AR-9511RG-R

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVS RMR GD-155 (+2MM L/H)
ARTHREX, INC.
AR-9511RG-L
In Commercial Distribution

  • 00888867061842 ()
AR-9511RG-L

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVS RMR GD-155 (NEUTRAL)
ARTHREX, INC.
AR-9511RG-C
In Commercial Distribution

  • 00888867061835 ()
AR-9511RG-C

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVS STEM/CUP INSERTR IMPACTOR
ARTHREX, INC.
AR-9511
In Commercial Distribution

  • 00888867061828 ()
AR-9511

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVS RMR GD-135 (+2MM R/H)
ARTHREX, INC.
AR-9510RG-R
In Commercial Distribution

  • 00888867061811 ()
AR-9510RG-R

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVS RMR GD-135 (+2MM L/H)
ARTHREX, INC.
AR-9510RG-L
In Commercial Distribution

  • 00888867061804 ()
AR-9510RG-L

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVS RMR GD-135 (NEUTRAL)
ARTHREX, INC.
AR-9510RG-C
In Commercial Distribution

  • 00888867061798 ()
AR-9510RG-C

  • Bone-resection orthopaedic reamer, reusable
UNIVERS REVERS RASP/TRIAL STEM- SIZE 15
ARTHREX, INC.
AR-9510-15
In Commercial Distribution

  • 00888867061781 ()
AR-9510-15

  • Bone file/rasp, manual, reusable
UNIVERS REVERS RASP/TRIAL STEM- SIZE 14
ARTHREX, INC.
AR-9510-14
In Commercial Distribution

  • 00888867061774 ()
AR-9510-14

  • Bone file/rasp, manual, reusable
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