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.DIAMOND BURR III D4.0MM
Aesculap AG
GE617SU
In Commercial Distribution

  • 04038653398904 ()
GE617SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR CRS.I D2.3MM
Aesculap AG
GE424SU
In Commercial Distribution

  • 04038653398898 ()
GE424SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR III D3.1MM
Aesculap AG
GE616SU
In Commercial Distribution

  • 04038653398881 ()
GE616SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR III D2.3MM
Aesculap AG
GE614SU
In Commercial Distribution

  • 04038653398874 ()
GE614SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR III D1.8MM
Aesculap AG
GE613SU
In Commercial Distribution

  • 04038653398850 ()
GE613SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR III D6.0MM
Aesculap AG
GE609SU
In Commercial Distribution

  • 04038653398843 ()
GE609SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR III D5.0MM
Aesculap AG
GE608SU
In Commercial Distribution

  • 04038653398836 ()
GE608SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR III D4.0MM
Aesculap AG
GE607SU
In Commercial Distribution

  • 04038653398829 ()
GE607SU

  • Orthopaedic bur, single-use
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.ROSEN BURR III D1.8MM
Aesculap AG
GE603SU
In Commercial Distribution

  • 04038653398782 ()
GE603SU

  • Orthopaedic bur, single-use
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