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 DIAM.NEURO CUTTER III D5.0MM
Aesculap AG
GE845SU
In Commercial Distribution

  • 04046963935245 ()
GE845SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER III D3.0MM
Aesculap AG
GE843SU
In Commercial Distribution

  • 04046963935238 ()
GE843SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.DIAMOND BURR II D3.0MM
Aesculap AG
GE816SU
In Commercial Distribution

  • 04046963935221 ()
GE816SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.DIAMOND BURR II D4.0MM
Aesculap AG
GE817SU
In Commercial Distribution

  • 04046963935214 ()
GE817SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER II D5.0MM
Aesculap AG
GE815SU
Not in Commercial Distribution

  • 04046963935207 ()
GE815SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER II D4.0MM
Aesculap AG
GE814SU
In Commercial Distribution

  • 04046963935191 ()
GE814SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER II D3.0MM
Aesculap AG
GE813SU
In Commercial Distribution

  • 04046963935184 ()
GE813SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.ROSEN BURR III D3.0MM
Aesculap AG
GE834SU
In Commercial Distribution

  • 04046963935177 ()
GE834SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.NEURO CUTTER III D3.0MM
Aesculap AG
GE833SU
Not in Commercial Distribution

  • 04046963935160 ()
GE833SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.NEURO CUTTER III D2.0MM
Aesculap AG
GE832SU
In Commercial Distribution

  • 04046963935153 ()
GE832SU

  • Orthopaedic bur, single-use
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