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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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Pituitary-5mm Straight
Seaspine Orthopedics Corporation
06-50-0123
In Commercial Distribution

  • 10889981104276 ()

  • 5mm
06-50-0123

  • Spinal rongeur
Pituitary-Straight 3mm
Seaspine Orthopedics Corporation
06-50-0121
In Commercial Distribution

  • 10889981104252 ()

  • 3mm
06-50-0121

  • Spinal rongeur
Cup-#3 Pull Rev Bayonetted
Seaspine Orthopedics Corporation
06-50-0114
In Commercial Distribution

  • 10889981104238 ()
06-50-0114

  • Bone curette, reusable
Cup-#3 Pull Fwd Bayonetted
Seaspine Orthopedics Corporation
06-50-0113
In Commercial Distribution

  • 10889981104221 ()
06-50-0113

  • Bone curette, reusable
Cup-#3 Right 30 Deg Bayonetted
Seaspine Orthopedics Corporation
06-50-0111
In Commercial Distribution

  • 10889981104207 ()

  • 30 Deg
06-50-0111

  • Bone curette, reusable
Curette-#1 Pull Rev Bayonetted
Seaspine Orthopedics Corporation
06-50-0104
In Commercial Distribution

  • 10889981104184 ()
06-50-0104

  • Bone curette, reusable
Curette- #1 Left 30 Deg Bayonetted
Seaspine Orthopedics Corporation
06-50-0102
In Commercial Distribution

  • 10889981104160 ()

  • 30 Deg
06-50-0102

  • Bone curette, reusable
Cup-#0 Fwd Bayonetted
Seaspine Orthopedics Corporation
06-50-0090
In Commercial Distribution

  • 10889981104115 ()
06-50-0090

  • Bone curette, reusable
Curette-#4/0 Pull Rev Bayonetted
Seaspine Orthopedics Corporation
06-50-0082
In Commercial Distribution

  • 10889981104108 ()
06-50-0082

  • Bone curette, reusable
Curette-#4/0 Fwd Bayonetted
Seaspine Orthopedics Corporation
06-50-0080
In Commercial Distribution

  • 10889981104085 ()
06-50-0080

  • Bone curette, reusable
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