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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,POST RESECT GD,6MM
ARTHREX, INC.
AR-601-PB06
In Commercial Distribution

  • 00888867037274 ()
AR-601-PB06

  • Suturing unit, single-use
IBAL UKA,POST RESECT GD,5MM
ARTHREX, INC.
AR-601-PB05
In Commercial Distribution

  • 00888867037267 ()
AR-601-PB05

  • Suturing unit, single-use
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
IBAL UKA,CHAMFER & PEG GD,SZ 6,RM/LL
ARTHREX, INC.
AR-601-CRMF
In Commercial Distribution

  • 00888867036994 ()
AR-601-CRMF

  • Arthroscopic shaver system blade, reusable
IBAL UKA,CHAMFER & PEG GD,SZ 5,RM/LL
ARTHREX, INC.
AR-601-CRME
In Commercial Distribution

  • 00888867036987 ()
AR-601-CRME

  • Bone lever/elevator, reusable
IBAL UKA,CHAMFER & PEG GD,SZ 4,RM/LL
ARTHREX, INC.
AR-601-CRMD
In Commercial Distribution

  • 00888867036970 ()
AR-601-CRMD

  • Bone lever/elevator, reusable
IBAL UKA,CHAMFER & PEG GD,SZ 3,RM/LL
ARTHREX, INC.
AR-601-CRMC
In Commercial Distribution

  • 00888867036963 ()
AR-601-CRMC

  • Orthopaedic fixation implant alignment tool
IBAL UKA,CHAMFER & PEG GD,SZ 2,RM/LL
ARTHREX, INC.
AR-601-CRMB
In Commercial Distribution

  • 00888867036956 ()
AR-601-CRMB

  • Suturing unit, reusable
IBAL UKA,CHAMFER & PEG GD,SZ 1,RM/LL
ARTHREX, INC.
AR-601-CRMA
In Commercial Distribution

  • 00888867036949 ()
AR-601-CRMA

  • Surgical instrument handle, non-torque-limiting
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