SEARCH RESULTS FOR: (*EPS Shape Moulding Machine*)(30990 results)

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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 Device Size Type Device Class Implantable

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HI-LINE XXS DISP.NEURO CUTTER III D2.0MM
Aesculap AG
GE832SU
In Commercial Distribution

  • 04046963935153 ()
GE832SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.ROSEN BURR II D3.0MM
Aesculap AG
GE804SU
In Commercial Distribution

  • 04046963935146 ()
GE804SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.NEURO CUTTER II D3.0MM
Aesculap AG
GE803SU
In Commercial Distribution

  • 04046963935139 ()
GE803SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.NEURO CUTTER II D2.0MM
Aesculap AG
GE802SU
In Commercial Distribution

  • 04046963935122 ()
GE802SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.DIAMOND BURR III D5.0MM
Aesculap AG
GE848SU
In Commercial Distribution

  • 04046964076800 ()
GE848SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER III D2.0MM
Aesculap AG
GE842SU
In Commercial Distribution

  • 04046964076695 ()
GE842SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.ROSEN BURR III D4.0MM
Aesculap AG
GE835SU
In Commercial Distribution

  • 04046964076688 ()
GE835SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.DIAMOND BURR II D5.0MM
Aesculap AG
GE818SU
In Commercial Distribution

  • 04046964076671 ()
GE818SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER II D2.0MM
Aesculap AG
GE812SU
In Commercial Distribution

  • 04046964076664 ()
GE812SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.ROSEN BURR II D4.0MM
Aesculap AG
GE805SU
In Commercial Distribution

  • 04046964076657 ()
GE805SU

  • Orthopaedic bur, single-use
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