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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SUREFIRE SCORPION NEEDLE
ARTHREX, INC.
AR-13991N
In Commercial Distribution

  • 00888867015920 ()
  • 10888867015927 ()
AR-13991N

  • Suturing needle, single-use
FLEXIBLE OSTETOME BLADE
ARTHREX, INC.
AR-13302F-35
In Commercial Distribution

  • 10888867010687 ()
  • 00888867010680 ()
AR-13302F-35

  • Orthopaedic osteotome blade, single-use
FLEXIBLE OSTETOME BLADE
ARTHREX, INC.
AR-13302F-25
In Commercial Distribution

  • 10888867010670 ()
  • 00888867010673 ()
AR-13302F-25

  • Orthopaedic osteotome blade, single-use
FLEXIBLE OSTETOME BLADE
ARTHREX, INC.
AR-13302F-10
In Commercial Distribution

  • 10888867010663 ()
  • 00888867010666 ()
AR-13302F-10

  • Orthopaedic osteotome blade, single-use
DISP INSTRS KIT FOR MINI S-TAK
ARTHREX, INC.
AR-1322DSC
In Commercial Distribution

  • 10888867010182 ()
  • 00888867010185 ()
AR-1322DSC

  • Arthroscopic surgical procedure kit, non-medicated, single-use
GUIDE PIN W/ SUTURE EYE 2.4 MM X 435 MM
ARTHREX, INC.
AR-1297LS
In Commercial Distribution

  • 00888867007239 ()
AR-1297LS

  • Fluted surgical drill bit, single-use
NDL,SUTRING,NIT W/WIRE LOOP END
ARTHREX, INC.
AR-1291S
In Commercial Distribution

  • 10888867007106 ()
  • 00888867007109 ()
AR-1291S

  • Suturing needle, single-use
NEEDLE, SUTURING, GRAFT PREPARATION
ARTHREX, INC.
AR-1291-4
In Commercial Distribution

  • 10888867007090 ()
  • 00888867007093 ()
AR-1291-4

  • Suturing needle, single-use
RETROPASSER
ARTHREX, INC.
AR-1259
In Commercial Distribution

  • 00888867006645 ()
AR-1259

  • Suturing unit, single-use
RETRODRILL GUIDE ASSEMBLY, CANNULATED
ARTHREX, INC.
AR-1250RP
In Commercial Distribution

  • 00888867006300 ()
AR-1250RP

  • Cannulated surgical drill bit, single-use
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