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 Type Device Class Implantable

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HI-LINE XS DISP.BARREL BURR III D6.0MM
Aesculap AG
GE646SU
In Commercial Distribution

  • 04038653399109 ()
GE646SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR II D1.8MM
Aesculap AG
GE503SU
In Commercial Distribution

  • 04038653399093 ()
GE503SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.BARREL BURR III D4.0MM
Aesculap AG
GE644SU
In Commercial Distribution

  • 04038653399086 ()
GE644SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR II D1.4MM
Aesculap AG
GE502SU
In Commercial Distribution

  • 04038653399079 ()
GE502SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER III D3.1MM
Aesculap AG
GE635SU
In Commercial Distribution

  • 04038653399062 ()
GE635SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR II D1.0MM
Aesculap AG
GE501SU
In Commercial Distribution

  • 04038653399055 ()
GE501SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER III D2.3MM
Aesculap AG
GE634SU
In Commercial Distribution

  • 04038653399048 ()
GE634SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ACORN BURR I D6.0MM
Aesculap AG
GE437SU
In Commercial Distribution

  • 04038653399031 ()
GE437SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR CRS.III D3.1MM
Aesculap AG
GE625SU
In Commercial Distribution

  • 04038653399000 ()
GE625SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TWIST DRILL I D2.0MM
Aesculap AG
GE433SU
In Commercial Distribution

  • 04038653398997 ()
GE433SU

  • Orthopaedic bur, single-use
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