SEARCH RESULTS FOR: arthrex*(8149 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 Class Implantable

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IBAL UKA,SPACER BLK MOD +,10MM
ARTHREX, INC.
AR-601-SM10
In Commercial Distribution

  • 00888867037397 ()
AR-601-SM10

  • Suturing unit, single-use
IBAL UKA,SPACER BLK MOD +,5MM
ARTHREX, INC.
AR-601-SM05
In Commercial Distribution

  • 00888867037380 ()
AR-601-SM05

  • Suturing unit, single-use
IBALANCE UKA, SPURRED HANDLE
ARTHREX, INC.
AR-601-SH00
In Commercial Distribution

  • 00888867037373 ()
AR-601-SH00

  • Electromechanical device/system transport trolley
IBALANCE UKA, SPACER BLOCK INSERT, 10MM
ARTHREX, INC.
AR-601-SB10
In Commercial Distribution

  • 00888867037366 ()
AR-601-SB10

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 9MM
ARTHREX, INC.
AR-601-SB09
In Commercial Distribution

  • 00888867037359 ()
AR-601-SB09

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 8MM
ARTHREX, INC.
AR-601-SB08
In Commercial Distribution

  • 00888867037342 ()
AR-601-SB08

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 7MM
ARTHREX, INC.
AR-601-SB07
In Commercial Distribution

  • 00888867037335 ()
AR-601-SB07

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK INSERT, 6MM
ARTHREX, INC.
AR-601-SB06
In Commercial Distribution

  • 00888867037328 ()
AR-601-SB06

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,10MM
ARTHREX, INC.
AR-601-PB10
In Commercial Distribution

  • 00888867037311 ()
AR-601-PB10

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,9MM
ARTHREX, INC.
AR-601-PB09
In Commercial Distribution

  • 00888867037304 ()
AR-601-PB09

  • Suturing unit, single-use
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