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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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DRILL GUIDE FOR H.T.O
ARTHREX, INC.
AR-13320
In Commercial Distribution

  • 00888867011243 ()
AR-13320

  • Surgical drill guide, reusable
CUTTING GUIDE FOR H.T.O.
ARTHREX, INC.
AR-13315
In Commercial Distribution

  • 00888867011205 ()
AR-13315

  • Osteotomy guide, reusable
ALIGNMENT ROD
ARTHREX, INC.
AR-13308
In Commercial Distribution

  • 00888867010802 ()
AR-13308

  • Fluted surgical drill bit, reusable
OSTEOTOMY PLATE CASE
ARTHREX, INC.
AR-13307P
In Commercial Distribution

  • 00888867010796 ()
AR-13307P

  • Device sterilization/disinfection container, reusable
OSTEOTOMY INST. STERILE CASE
ARTHREX, INC.
AR-13307
In Commercial Distribution

  • 00888867010789 ()
AR-13307

  • Device sterilization/disinfection container, reusable
OSTEOTOMY CUTTING GUIDE
ARTHREX, INC.
AR-13306-01
In Commercial Distribution

  • 00888867010765 ()
AR-13306-01

  • Osteotomy guide, reusable
OSTEOTOMY GUIDE ASSEMBLY
ARTHREX, INC.
AR-13305
In Commercial Distribution

  • 00888867010758 ()
AR-13305

  • Osteotomy guide, reusable
GUIDE SLEEVE PARALLEL
ARTHREX, INC.
AR-13304-2
In Commercial Distribution

  • 00888867010741 ()
AR-13304-2

  • Orthopaedic implantation sleeve, reusable
GUIDE SLEEVE BODY PARALLEL
ARTHREX, INC.
AR-13304-1
In Commercial Distribution

  • 00888867010734 ()
AR-13304-1

  • Orthopaedic implantation sleeve, reusable
FLEXIBLE OSTETOME BLADE
ARTHREX, INC.
AR-13302F-35
In Commercial Distribution

  • 10888867010687 ()
  • 00888867010680 ()
AR-13302F-35

  • Orthopaedic osteotome blade, single-use
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