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.ROSEN BURR III D2.3MM
Aesculap AG
GE604SU
In Commercial Distribution

  • 04038653398805 ()
GE604SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.CRANIOTOME CUTTER I
Aesculap AG
GE420SU
In Commercial Distribution

  • 04038653398744 ()
GE420SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.CONE BURR II D4.0MM
Aesculap AG
GE540SU
In Commercial Distribution

  • 04038653398720 ()
GE540SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ACORN BURR II D6.0MM
Aesculap AG
GE537SU
In Commercial Distribution

  • 04038653398713 ()
GE537SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D6.0MM
Aesculap AG
GE419SU
In Commercial Distribution

  • 04038653398706 ()
GE419SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER II D3.1MM
Aesculap AG
GE535SU
In Commercial Distribution

  • 04038653398690 ()
GE535SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D5.0MM
Aesculap AG
GE418SU
In Commercial Distribution

  • 04038653398683 ()
GE418SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER II D2.3MM
Aesculap AG
GE534SU
In Commercial Distribution

  • 04038653398676 ()
GE534SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D4.0MM
Aesculap AG
GE417SU
In Commercial Distribution

  • 04038653398669 ()
GE417SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TWIST DRILL II D2.0MM
Aesculap AG
GE533SU
In Commercial Distribution

  • 04038653398652 ()
GE533SU

  • Orthopaedic bur, single-use
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