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.PIN PT.CUTT./GB740R D1.0
Aesculap AG
GE392SU
In Commercial Distribution

  • 04046963145903 ()
GE392SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR/GB740R D3.1
Aesculap AG
GE394SU
In Commercial Distribution

  • 04046963117900 ()
GE394SU

  • 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
HI-LINE XS DISP.NEURO CUTTER III+ D3.1MM
Aesculap AG
GE655SU
In Commercial Distribution

  • 04046963086725 ()
GE655SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER III D3.1MM
Aesculap AG
GE654SU
Not in Commercial Distribution

  • 04046963086701 ()
GE654SU

  • 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.DIAMOND BURR XL-3 D4.5MM
Aesculap AG
GE296SU
In Commercial Distribution

  • 04046963519216 ()
GE296SU

  • Orthopaedic bur, single-use
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