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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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Interbody, 31mm X 24mm X 18mm, 20 Deg, 3D
Seaspine Orthopedics Corporation
WA4-101820
In Commercial Distribution

  • 10889981304942 ()
WA4-101820

  • Metallic spinal interbody fusion cage
Interbody, 39mm x 30mm x 16mm, 20 Deg, 3D
Seaspine Orthopedics Corporation
WA4-131620
In Commercial Distribution

  • 10889981303686 ()
WA4-131620

  • Metallic spinal interbody fusion cage
Interbody, 35mm x 27mm x 18mm, 20 Deg, 3D
Seaspine Orthopedics Corporation
WA4-111820
In Commercial Distribution

  • 10889981303570 ()
WA4-111820

  • Metallic spinal interbody fusion cage
Interbody, 31mm x 24mm x 16mm, 20 Deg, 3D
Seaspine Orthopedics Corporation
WA4-101620
In Commercial Distribution

  • 10889981303457 ()
WA4-101620

  • Metallic spinal interbody fusion cage
F3D Lateral 22mm x 60mm x 18mm x 20°
CORELINK LLC
3LL2260-2018
In Commercial Distribution

  • M7253LL22602018 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 60mm x 16mm x 20°
CORELINK LLC
3LL2260-2016
In Commercial Distribution

  • M7253LL22602016 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 60mm x 14mm x 20°
CORELINK LLC
3LL2260-2014
In Commercial Distribution

  • M7253LL22602014 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 22mm x 60mm x 12mm x 20°
CORELINK LLC
3LL2260-2012
In Commercial Distribution

  • M7253LL22602012 ()


  • Spinal fixation plate, non-bioabsorbable
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
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