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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, 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
Angled Distractor Tip, 20°, 18mm
Altus Spine, LLC
1030-2018
In Commercial Distribution

  • 00843210171364 ()


  • Orthopaedic surgical distractor, internal
Angled Distractor Tip, 20°, 17mm
Altus Spine, LLC
1030-2017
In Commercial Distribution

  • 00843210171357 ()


  • Orthopaedic surgical distractor, internal
Angled Distractor Tip, 20°, 16mm
Altus Spine, LLC
1030-2016
In Commercial Distribution

  • 00843210171340 ()


  • Orthopaedic surgical distractor, internal
Angled Distractor Tip, 20°, 14mm
Altus Spine, LLC
1030-2014
In Commercial Distribution

  • 00843210171326 ()


  • Orthopaedic surgical distractor, internal
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242013T
In Commercial Distribution

  • 00843210161532 ()


  • Polymeric spinal interbody fusion cage
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