SEARCH RESULTS FOR: 怎么做假AT(5634 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 Type Device Class Implantable

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HI-LINE XS DISP.DIAMOND BURR I D0.8MM
Aesculap AG
GE460SU
In Commercial Distribution

  • 04046963816223 ()
GE460SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D0.6MM
Aesculap AG
GE459SU
In Commercial Distribution

  • 04046963816216 ()
GE459SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR X-CRS.I D5.0MM
Aesculap AG
GE457SU
In Commercial Distribution

  • 04046963816209 ()
GE457SU

  • Orthopaedic bur, single-use
HI-LINE XXS DIAM.NEURO CUTTER III D4.0MM
Aesculap AG
GE844SU
In Commercial Distribution

  • 04046963935269 ()
GE844SU

  • Orthopaedic bur, single-use
HI-LINE XXS DISP.DIAMOND BURR III D4.0MM
Aesculap AG
GE847SU
In Commercial Distribution

  • 04046963935252 ()
GE847SU

  • 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 D4.0MM
Aesculap AG
GE814SU
In Commercial Distribution

  • 04046963935191 ()
GE814SU

  • 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
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
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