SEARCH RESULTS FOR: arthrex*(17270 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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COMPRESSION FT SCREW SYS CADDY, STANDARD
ARTHREX, INC.
AR-8738C-04
In Commercial Distribution

  • 00888867127418 ()
AR-8738C-04

  • Device sterilization/disinfection container, reusable
COMPRESSION FT SCREW SYS CADDY, MINI
ARTHREX, INC.
AR-8738C-03
In Commercial Distribution

  • 00888867127401 ()
AR-8738C-03

  • Device sterilization/disinfection container, reusable
COMPRESSION FT SCREW SYS CADDY, MICRO
ARTHREX, INC.
AR-8738C-02
In Commercial Distribution

  • 00888867127395 ()
AR-8738C-02

  • Device sterilization/disinfection container, reusable
COMPR FT SCRW SYS CADDY,COMMON INST
ARTHREX, INC.
AR-8738C-01
In Commercial Distribution

  • 00888867127388 ()
AR-8738C-01

  • Device sterilization/disinfection container, reusable
COMPRESSION FT SCREW SYS INSTRUMENT CASE
ARTHREX, INC.
AR-8738C
In Commercial Distribution

  • 00888867127371 ()
AR-8738C

  • Device sterilization/disinfection container, reusable
QCKFIX CANN SCRW SYS GENERAL INSERT
ARTHREX, INC.
AR-8737C-02
In Commercial Distribution

  • 00888867127333 ()
AR-8737C-02

  • Device sterilization/disinfection container, reusable
QCKFIX CANN SCRW SYS MICRO/MINI INSERT
ARTHREX, INC.
AR-8737C-01
In Commercial Distribution

  • 00888867127326 ()
AR-8737C-01

  • Device sterilization/disinfection container, reusable
PERC PIN CLAMP
ARTHREX, INC.
AR-8737-57
Not in Commercial Distribution

  • 00888867127319 ()
AR-8737-57

  • Suturing unit, reusable
GUIDE WIRE PLUNGER
ARTHREX, INC.
AR-8737-56
In Commercial Distribution

  • 00888867127302 ()
AR-8737-56

  • Orthopaedic implant impactor, reusable
PARALLEL GUIDE STANDARD CMP FT
ARTHREX, INC.
AR-8737-55
In Commercial Distribution

  • 00888867127296 ()
AR-8737-55

  • Surgical drill guide, reusable
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