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.TC ROSEN BURR II D5.0MM
Aesculap AG
GE508TC-SU
In Commercial Distribution

  • 04046963187057 ()
GE508TC-SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TC ROSEN BURR I D5.0MM
Aesculap AG
GE408TC-SU
Not in Commercial Distribution

  • 04046963187040 ()
GE408TC-SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TC ROSEN BURR III D4.0MM
Aesculap AG
GE607TC-SU
In Commercial Distribution

  • 04046963187026 ()
GE607TC-SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TC ROSEN BURR II D4.0MM
Aesculap AG
GE507TC-SU
In Commercial Distribution

  • 04046963187019 ()
GE507TC-SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TC ROSEN BURR I D4.0MM
Aesculap AG
GE407TC-SU
Not in Commercial Distribution

  • 04046963187002 ()
GE407TC-SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER III D1.8MM
Aesculap AG
GE631SU
In Commercial Distribution

  • 04046963129187 ()
GE631SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER II D1.8MM
Aesculap AG
GE531SU
Not in Commercial Distribution

  • 04046963129163 ()
GE531SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER I D3.1MM
Aesculap AG
GE435SU
In Commercial Distribution

  • 04046963129149 ()
GE435SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER I D2.3MM
Aesculap AG
GE434SU
Not in Commercial Distribution

  • 04046963129132 ()
GE434SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER III+ D3.1MM
Aesculap AG
GE653SU
In Commercial Distribution

  • 04046963086749 ()
GE653SU

  • Orthopaedic bur, single-use
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