SEARCH RESULTS FOR: arthrex*(9765 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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IBAL UKA,TIB SIZING GD,SZ 4,LM
ARTHREX, INC.
AR-601-TTL4
In Commercial Distribution

  • 00888867037960 ()
AR-601-TTL4

  • Suturing unit, single-use
IBAL UKA,TIB SIZING GD,SZ 1,LM
ARTHREX, INC.
AR-601-TTL1
In Commercial Distribution

  • 00888867037939 ()
AR-601-TTL1

  • Suturing unit, single-use
iBALANCE UKA, TIBIAL STYLUS, 0MM
ARTHREX, INC.
AR-601-TS00
In Commercial Distribution

  • 00888867037915 ()
AR-601-TS00

  • Suturing unit, single-use
iBALANCE UKA, RESECTION GUIDE, RIGHT
ARTHREX, INC.
AR-601-TRRM
In Commercial Distribution

  • 00888867037908 ()
AR-601-TRRM

  • Device sterilization/disinfection container, reusable
iBALANCE UKA, RESECTION GUIDE, LEFT
ARTHREX, INC.
AR-601-TRLM
In Commercial Distribution

  • 00888867037892 ()
AR-601-TRLM

  • Device sterilization/disinfection container, reusable
UNI-KNEE TIBIA PEG DRILL DIA. .312
ARTHREX, INC.
AR-601-TPD0
In Commercial Distribution

  • 00888867037885 ()
AR-601-TPD0

  • Suturing unit, single-use
iBALANCE UKA, TIBIAL KEEL PUNCH
ARTHREX, INC.
AR-601-TKBR
In Commercial Distribution

  • 00888867037861 ()
AR-601-TKBR

  • Device sterilization/disinfection container, reusable
iBALANCE UKA TIBIAL IMP- ACTOR HEAD
ARTHREX, INC.
AR-601-TIH0
In Commercial Distribution

  • 00888867037854 ()
AR-601-TIH0

  • Orthopaedic surgical distractor, internal
iBALANCE UKA TIBIAL IMP- ACTOR BODY ASSY
ARTHREX, INC.
AR-601-TIB0
In Commercial Distribution

  • 00888867037847 ()
AR-601-TIB0

  • Orthopaedic surgical distractor, internal
iBALANCE UKA, TIBIAL ALIGNMENT GUIDE
ARTHREX, INC.
AR-601-TG00
In Commercial Distribution

  • 00888867037830 ()
AR-601-TG00

  • Suturing unit, single-use
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