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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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ANKLE FUSION CADDY POLYPRO REPLACEMENT
ARTHREX, INC.
AR-8970C-SC-01
Not in Commercial Distribution

  • 00888867198333 ()
AR-8970C-SC-01

  • Device sterilization/disinfection container, reusable
Joint Space Guide
ARTHREX, INC.
AR-10200
In Commercial Distribution

  • 00888867195486 ()
AR-10200

  • Surgical drill guide, reusable
INST. CASE, NAUTILUS REAMER
ARTHREX, INC.
AR-9216NRC
In Commercial Distribution

  • 00888867195318 ()
AR-9216NRC

  • Device sterilization/disinfection container, reusable
ANKLE FUSION PLATING INSTRUMENT CASE
ARTHREX, INC.
AR-8970C
In Commercial Distribution

  • 00888867195028 ()
AR-8970C

  • Device sterilization/disinfection container, reusable
DRIVER, T8 HEXALOBE SELF RETAINING
ARTHREX, INC.
AR-8916-27
In Commercial Distribution

  • 00888867177628 ()
AR-8916-27

  • Orthopaedic inorganic implant inserter/extractor, reusable
Suture Cutter, Top Release
ARTHREX, INC.
SP-12250-1
In Commercial Distribution

  • 00888867175136 ()
SP-12250-1

  • General-purpose surgical scissors, reusable
UNIVERS REVS REVISION SSTEM INSTR CS
ARTHREX, INC.
AR-9501RHC
In Commercial Distribution

  • 00888867140462 ()
AR-9501RHC

  • Device sterilization/disinfection container, reusable
UNIVERS REVERS SCREW CADDY
ARTHREX, INC.
AR-9501GC-SC
In Commercial Distribution

  • 00888867140370 ()
AR-9501GC-SC

  • Device sterilization/disinfection container, reusable
UNIVERS REVERS GLENOID INSTRUMENT CASE
ARTHREX, INC.
AR-9501GC
In Commercial Distribution

  • 00888867140363 ()
AR-9501GC

  • Device sterilization/disinfection container, reusable
INTRAMEDULLARY HUMERAL CUTTING GUIDE
ARTHREX, INC.
AR-9401-14
In Commercial Distribution

  • 00888867139640 ()
AR-9401-14

  • Surgical depth gauge, reusable
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