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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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No Description
Biomet Orthopedics, LLC
03090
In Commercial Distribution

  • 00887868081804 ()
03090

  • Orthopaedic implantation sleeve, reusable
No Description
Biomet Orthopedics, LLC
03085
In Commercial Distribution

  • 00887868081798 ()
03085

  • Orthopaedic implantation sleeve, reusable
No Description
Biomet Orthopedics, LLC
03080
In Commercial Distribution

  • 00887868081781 ()
03080

  • Orthopaedic implantation sleeve, reusable
No Description
Biomet Orthopedics, LLC
03075
In Commercial Distribution

  • 00887868081774 ()
03075

  • Orthopaedic trocar blade, reusable
No Description
Biomet Orthopedics, LLC
03070
In Commercial Distribution

  • 00887868081767 ()
03070

  • Surgical drill guide, reusable
No Description
Biomet Orthopedics, LLC
03065
In Commercial Distribution

  • 00887868081750 ()
3065

  • Surgical drill guide, reusable
No Description
Biomet Orthopedics, LLC
03060
In Commercial Distribution

  • 00887868081743 ()
03060

  • Surgical drill guide, reusable
No Description
Biomet Orthopedics, LLC
01227
In Commercial Distribution

  • 00887868080845 ()
01227

  • Surgical torque wrench, reusable
X SERIES MONITOR/DEFIBRILLATOR 12 LEAD/W INTERP, PACING, NIBP, SPO2, SPCO, IBP/TEMP CPR EXPANSION PACK AND ETCO2, DMST, REFURB, (TIER 4, CONTAINS 610)
Zoll Medical Corporation
601-2231511-01-664
In Commercial Distribution

  • 00812394026272 ()


  • Rechargeable professional automated external defibrillator
DEVICE IDENTIFIER, X SERIES MONITOR/DEFIBRILLATOR W/PACING, 12 LEAD W/INTERP, SPO2, NIBP, IBP/TEMP, CPR EXPANSION PACK, ETCO2, DMST, REFURB (TIER 4, CONTAINS 610)
Zoll Medical Corporation
601-2221511-01-664
In Commercial Distribution

  • 00812394026265 ()


  • Rechargeable professional automated external defibrillator
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