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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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Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272018T
In Commercial Distribution

  • 00843210181073 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272019T
In Commercial Distribution

  • 00843210181066 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 38mmx27mm
Altus Spine, LLC
SL38272020T
In Commercial Distribution

  • 00843210181059 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302015T
In Commercial Distribution

  • 00843210180182 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302016T
In Commercial Distribution

  • 00843210180175 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302017T
In Commercial Distribution

  • 00843210180168 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302018T
In Commercial Distribution

  • 00843210180151 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302019T
In Commercial Distribution

  • 00843210180144 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 42mmx30mm
Altus Spine, LLC
SL42302020T
In Commercial Distribution

  • 00843210180137 ()


  • Polymeric spinal interbody fusion cage
Angled Distractor Tip, 20°, 20mm
Altus Spine, LLC
1030-2020
In Commercial Distribution

  • 00843210171388 ()


  • Orthopaedic surgical distractor, internal
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