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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, 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, 37.5mm DB Pre-Bent
Nuvasive, Inc.
7237375
In Commercial Distribution

  • 00887517439000 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 35mm DB Pre-Bent
Nuvasive, Inc.
7237350
In Commercial Distribution

  • 00887517438690 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 32.5mm DB Pre-Bent
Nuvasive, Inc.
7237325
In Commercial Distribution

  • 00887517438683 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 30mm DB Pre-Bent
Nuvasive, Inc.
7237300
In Commercial Distribution

  • 00887517438676 ()


  • Bone-screw internal spinal fixation system rod
SpheRx® DBR® III Rod, 27.5mm DB Pre-Bent
Nuvasive, Inc.
7237275
In Commercial Distribution

  • 00887517438669 ()


  • Bone-screw internal spinal fixation system rod
No Description
SDI LIMITED
AURA 20 COMP DB
Not in Commercial Distribution

  • DO3685650111 ()
  • DO3685650110 ()
8565011

  • Dental unfilled resin sealant/coating
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