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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GUIDE WIRE, 2 MM X 150 MM, STRL.
ARTHREX, INC.
AR-8945KS
In Commercial Distribution

  • 00888867247079 ()
AR-8945KS

  • Suturing unit, single-use
GUIDE WIRE, THRDED, 1.35 MM x 150 MM, ST
ARTHREX, INC.
AR-8943-38S
In Commercial Distribution

  • 00888867247062 ()
AR-8943-38S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, 1.35 MM X 150 MM, STRL
ARTHREX, INC.
AR-8943-01S
In Commercial Distribution

  • 00888867247055 ()
AR-8943-01S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, 1.14 MM X 150 MM , STRL
ARTHREX, INC.
AR-8933KS
In Commercial Distribution

  • 00888867247024 ()
AR-8933KS

  • Suturing unit, single-use
GUIDE WIRE, 0.86 MM X 95 MM, STRL
ARTHREX, INC.
AR-8737-21S
In Commercial Distribution

  • 00888867246935 ()
AR-8737-21S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, THRDED, 1.1 MM X 120 MM, STR
ARTHREX, INC.
AR-8737-05S
In Commercial Distribution

  • 00888867246928 ()
AR-8737-05S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, THRDED, 1.35 MM X 150 MM STR
ARTHREX, INC.
AR-8737-02S
In Commercial Distribution

  • 00888867246904 ()
AR-8737-02S

  • Fluted surgical drill bit, single-use
GUIDE WIRE, 1 MM X 95 MM, STRL
ARTHREX, INC.
AR-8708KS
In Commercial Distribution

  • 00888867246881 ()
AR-8708KS

  • Fluted surgical drill bit, single-use
GUIDE WIRE, 1.14 MM X 203 MM, STRL
ARTHREX, INC.
AR-5025KS
In Commercial Distribution

  • 00888867246805 ()
AR-5025KS

  • Suturing unit, single-use
GUIDE WIRE, 2 MM X 305 MM, STRL
ARTHREX, INC.
AR-4202S
In Commercial Distribution

  • 00888867246751 ()
AR-4202S

  • Suturing unit, single-use
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