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,POST RESECT GD,4MM
ARTHREX, INC.
AR-601-PB04
In Commercial Distribution

  • 00888867037250 ()
AR-601-PB04

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,3MM
ARTHREX, INC.
AR-601-PB03
In Commercial Distribution

  • 00888867037243 ()
AR-601-PB03

  • Suturing unit, single-use
IBALANCE UKA, SPACER BLOCK HANDLE ASSY
ARTHREX, INC.
AR-601-KSBH
In Commercial Distribution

  • 00888867037236 ()
AR-601-KSBH

  • Orthopaedic prosthesis implantation positioning instrument, reusable
IBALANCE UKA, FEMORAL TRIAL, SZ 6, RM/LL
ARTHREX, INC.
AR-601-FTRF
In Commercial Distribution

  • 00888867037229 ()
AR-601-FTRF

  • Knee femur prosthesis trial, reusable
IBALANCE UKA, FEMORAL TRIAL, SZ 5, RM/LL
ARTHREX, INC.
AR-601-FTRE
In Commercial Distribution

  • 00888867037212 ()
AR-601-FTRE

  • Knee femur prosthesis trial, reusable
IBALANCE UKA, FEMORAL TRIAL, SZ 4, RM/LL
ARTHREX, INC.
AR-601-FTRD
In Commercial Distribution

  • 00888867037205 ()
AR-601-FTRD

  • Knee femur prosthesis trial, reusable
IBALANCE UKA, FEMORAL TRAIL, SZ 3, RM/LL
ARTHREX, INC.
AR-601-FTRC
In Commercial Distribution

  • 00888867037199 ()
AR-601-FTRC

  • Knee femur prosthesis trial, reusable
IBALANCE UKA, FEMORAL TRAIL, SZ 2, RM/LL
ARTHREX, INC.
AR-601-FTRB
In Commercial Distribution

  • 00888867037182 ()
AR-601-FTRB

  • Knee femur prosthesis trial, reusable
IBALANCE UKA, FEMORAL TRIAL, SZ 1, RM/LL
ARTHREX, INC.
AR-601-FTRA
In Commercial Distribution

  • 00888867037175 ()
AR-601-FTRA

  • Knee femur prosthesis trial, reusable
IBALANCE UKA, FEMORAL TRAIL, SZ 6, LM/RL
ARTHREX, INC.
AR-601-FTLF
In Commercial Distribution

  • 00888867037168 ()
AR-601-FTLF

  • Knee femur prosthesis trial, reusable
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