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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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iBALANCE, PATELLA CALIPERS
ARTHREX, INC.
AR-602-48
In Commercial Distribution

  • 00888867038417 ()
AR-602-48

  • Surgical implant/trial-implant/sizer holder, reusable
iBALANCE PATELLA DRILL GUIDE, 37MM
ARTHREX, INC.
AR-602-47
In Commercial Distribution

  • 00888867038400 ()
AR-602-47

  • Surgical drill guide, reusable
iBALANCE PATELLA DRILL GUIDE, 30MM
ARTHREX, INC.
AR-602-45
In Commercial Distribution

  • 00888867038387 ()
AR-602-45

  • Surgical drill guide, reusable
IBAL PFJ,PEG DRL STABILIZER SZ 4
ARTHREX, INC.
AR-602-41
In Commercial Distribution

  • 00888867038349 ()
AR-602-41

  • Surgical drill guide, reusable
IBAL PATLOFEM TRL,SZ 3,RT
ARTHREX, INC.
AR-602-3R
In Commercial Distribution

  • 00888867038325 ()
AR-602-3R

  • 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, 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
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
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