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 XXS DISP.NEURO CUTTER II D2.0MM
Aesculap AG
GE802SU
In Commercial Distribution

  • 04046963935122 ()
GE802SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.III D6.0
Aesculap AG
GE658SU
In Commercial Distribution

  • 04046963816445 ()
GE658SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.III D5.0
Aesculap AG
GE657SU
In Commercial Distribution

  • 04046963816438 ()
GE657SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.III D4.0
Aesculap AG
GE656SU
In Commercial Distribution

  • 04046963816421 ()
GE656SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR II+ D2.3MM
Aesculap AG
GE574SU
Not in Commercial Distribution

  • 04046963816414 ()
GE574SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.II D6.0
Aesculap AG
GE558SU
In Commercial Distribution

  • 04046963816339 ()
GE558SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.II D5.0
Aesculap AG
GE557SU
In Commercial Distribution

  • 04046963816322 ()
GE557SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.II D4.0
Aesculap AG
GE556SU
In Commercial Distribution

  • 04046963816315 ()
GE556SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR I+ D2.7MM
Aesculap AG
GE475SU
In Commercial Distribution

  • 04046963816285 ()
GE475SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR I+ D1.8MM
Aesculap AG
GE473SU
In Commercial Distribution

  • 04046963816278 ()
GE473SU

  • Orthopaedic bur, single-use
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