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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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Lordotic Scoring Trial, 10 mm x 15.5 mm x 14 mm (Modular)
Spine Wave, Inc.
10-9041
In Commercial Distribution

  • 10840642129533 ()
10-9041

  • Spinal implant trial
Lordotic Scoring Trial, 8 mm x 15.5 mm x 14 mm (Modular)
Spine Wave, Inc.
10-9039
In Commercial Distribution

  • 10840642129519 ()
10-9039

  • Spinal implant trial
Lordotic Scoring Trial, 6 mm x 15.5 mm x 14 mm (Modular)
Spine Wave, Inc.
10-9037
In Commercial Distribution

  • 10840642129496 ()
10-9037

  • Spinal implant trial
Anatomic Scoring Trial, 8 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5632
In Commercial Distribution

  • 10840642121063 ()
10-5632

  • Spinal implant trial
Anatomic Scoring Trial, 7 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5631
In Commercial Distribution

  • 10840642121056 ()
10-5631

  • Spinal implant trial
Anatomic Scoring Trial, 6 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5630
In Commercial Distribution

  • 10840642121049 ()
10-5630

  • Spinal implant trial
Anatomic Scoring Trial, 5 mm x 14 mm x 12 mm
Spine Wave, Inc.
10-5629
In Commercial Distribution

  • 10840642121032 ()
10-5629

  • Spinal implant trial
Anatomic Scoring Trial, 5 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5615
In Commercial Distribution

  • 10840642119060 ()
10-5615

  • Spinal implant trial
Anatomic Scoring Trial, 6 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5616
In Commercial Distribution

  • 10840642119053 ()
10-5616

  • Spinal implant trial
Anatomic Scoring Trial, 7 mm x 15.5 mm x 14 mm
Spine Wave, Inc.
10-5617
In Commercial Distribution

  • 10840642119046 ()
10-5617

  • Spinal implant trial
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