SEARCH RESULTS FOR: arthrex*(9019 results)

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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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iBal TKA Lock Fem Impact, Replace Bumper
ARTHREX, INC.
AR-613-49RB
In Commercial Distribution

  • 00888867284371 ()
AR-613-49RB

  • Orthopaedic implant impactor, reusable
iBalance TKA Locking Femoral Impactor
ARTHREX, INC.
AR-613-49NT
Not in Commercial Distribution

  • 00888867284364 ()
AR-613-49NT

  • Orthopaedic implant impactor, reusable
PASSPORT BUTTON CANNULA
ARTHREX, INC.
AR-6592-10-20-1
In Commercial Distribution

  • 00888867284319 ()
AR-6592-10-20-1

  • Arthroscopic access cannula, single-use
PASSPORT BUTTON CANNULA
ARTHREX, INC.
AR-6592-10-40-1
In Commercial Distribution

  • 00888867284302 ()
AR-6592-10-40-1

  • Arthroscopic access cannula, single-use
PASSPORT BUTTON CANNULA
ARTHREX, INC.
AR-6592-08-50-1
In Commercial Distribution

  • 00888867284289 ()
AR-6592-08-50-1

  • Bone access cannula
PASSPORT BUTTON CANNULA
ARTHREX, INC.
AR-6592-06-40-1
In Commercial Distribution

  • 00888867284265 ()
AR-6592-06-40-1

  • Arthroscopic access cannula, single-use
PASSPORT BUTTON CANNULA
ARTHREX, INC.
AR-6592-06-30-1
In Commercial Distribution

  • 00888867284258 ()
AR-6592-06-30-1

  • Bone access cannula
PASSPORT BUTTON CANNULA
ARTHREX, INC.
AR-6592-06-20-1
In Commercial Distribution

  • 00888867284241 ()
AR-6592-06-20-1

  • Arthroscopic access cannula, single-use
MULTIFIRE SCORPION NEEDLE
ARTHREX, INC.
AR-13995N-1
In Commercial Distribution

  • 00888867283985 ()
AR-13995N-1

  • Suturing unit, single-use
SUREFIRE SCORPION NEEDLE
ARTHREX, INC.
AR-13991N-1
In Commercial Distribution

  • 00888867283978 ()
AR-13991N-1

  • Suturing unit, single-use
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