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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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SpheRx® DBR® III Rod, 50mm DB Pre-Bent
Nuvasive, Inc.
7237500
In Commercial Distribution

  • 00887517439055 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 47.5mm DB Pre-Bent
Nuvasive, Inc.
7237475
In Commercial Distribution

  • 00887517439048 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 45mm DB Pre-Bent
Nuvasive, Inc.
7237450
In Commercial Distribution

  • 00887517439031 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 42.5mm DB Pre-Bent
Nuvasive, Inc.
7237425
In Commercial Distribution

  • 00887517439024 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 40mm DB Pre-Bent
Nuvasive, Inc.
7237400
In Commercial Distribution

  • 00887517439017 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 70.0mm DB Pre-Bent
Nuvasive, Inc.
7237700
In Commercial Distribution

  • 00887517439437 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 67.5mm DB Pre-Bent
Nuvasive, Inc.
7237675
In Commercial Distribution

  • 00887517439420 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 65.0mm DB Pre-Bent
Nuvasive, Inc.
7237650
In Commercial Distribution

  • 00887517439413 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 62.5mm DB Pre-Bent
Nuvasive, Inc.
7237625
In Commercial Distribution

  • 00887517439406 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 60.0mm DB Pre-Bent
Nuvasive, Inc.
7237600
In Commercial Distribution

  • 00887517439093 ()


  • Bone-screw internal spinal fixation system rod
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