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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-Profile Interbody, 31mm x 24mm x 16mm, 20 Deg
Seaspine Orthopedics Corporation
RA1-201620
In Commercial Distribution

  • 10889981246952 ()
RA1-201620

  • Metal-polymer composite spinal interbody fusion cage
No-Profile Interbody, 31mm x 24mm x 12mm, 20 Deg
Seaspine Orthopedics Corporation
RA1-201220
In Commercial Distribution

  • 10889981246938 ()
RA1-201220

  • Metal-polymer composite spinal interbody fusion cage
F3D Lateral 22mm x 55mm x 18mm x 20°
CORELINK LLC
3LL2255-2018
In Commercial Distribution

  • M7253LL22552018 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 55mm x 16mm x 20°
CORELINK LLC
3LL2255-2016
In Commercial Distribution

  • M7253LL22552016 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 55mm x 14mm x 20°
CORELINK LLC
3LL2255-2014
In Commercial Distribution

  • M7253LL22552014 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 55mm x 12mm x 20°
CORELINK LLC
3LL2255-2012
In Commercial Distribution

  • M7253LL22552012 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 50mm x 18mm x 20°
CORELINK LLC
3LL2250-2018
In Commercial Distribution

  • M7253LL22502018 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 50mm x 16mm x 20°
CORELINK LLC
3LL2250-2016
In Commercial Distribution

  • M7253LL22502016 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 50mm x 14mm x 20°
CORELINK LLC
3LL2250-2014
In Commercial Distribution

  • M7253LL22502014 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 50mm x 12mm x 20°
CORELINK LLC
3LL2250-2012
In Commercial Distribution

  • M7253LL22502012 ()


  • Spinal fixation plate, non-bioabsorbable
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