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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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3.8mm x 25-30mm
INTERVENTIONAL SPINE, INC
CS-38-2530
In Commercial Distribution

  • 81195401030024 ()
9031-04

  • Bone-screw internal spinal fixation system, sterile
3.8mm x 20-25mm
INTERVENTIONAL SPINE, INC
CS-38-2025
In Commercial Distribution

  • 81195401029448 ()
9031-03

  • Bone-screw internal spinal fixation system, sterile
3.8mm x 15-20mm
INTERVENTIONAL SPINE, INC
CS-38-1520
In Commercial Distribution

  • 81195401028762 ()
9031-02

  • Bone-screw internal spinal fixation system, sterile
3.8mm x 12-15mm
INTERVENTIONAL SPINE, INC
CS-38-1215
In Commercial Distribution

  • 81195401027086 ()
9031-01

  • Bone-screw internal spinal fixation system, sterile
PERPOS FCD-2 Stabilizer, 4.5mm I. D. x 10mm O. D.
INTERVENTIONAL SPINE, INC
9062
In Commercial Distribution

  • 81195401020124 ()
9062-00

  • Bone-screw internal spinal fixation system, sterile
PERPOS FCD-2 Anchor, 4.5mm Diameter by 37-44mm Length
INTERVENTIONAL SPINE, INC
9063-01
In Commercial Distribution

  • 81195401019548 ()
9063-01

  • Bone-screw internal spinal fixation system, sterile
PERPOS FCD-2 Anchor, 4.5mm Diameter by 28-35mm Length
INTERVENTIONAL SPINE, INC
9063-00
In Commercial Distribution

  • 81195401018862 ()
9063-00

  • Bone-screw internal spinal fixation system, sterile
2 Bone-Lok PLS Implant
INTERVENTIONAL SPINE, INC
9045-02
Not in Commercial Distribution

  • 81195401005824 ()
9045-02

  • Bone-screw internal spinal fixation system, sterile
4.5mm O.D. x 30-40mm Length
INTERVENTIONAL SPINE, INC
LSW-45-3040
Not in Commercial Distribution

  • 81195401002786 ()
9024-00

  • Bone-screw internal spinal fixation system, sterile
1 Bone-Lok PLS Implant
INTERVENTIONAL SPINE, INC
9045-01
Not in Commercial Distribution

  • 81195401000324 ()
9045-01

  • Bone-screw internal spinal fixation system, sterile
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