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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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Connector, Parallel, O-U, Double, Medium
Spine Wave, Inc.
11-7411
In Commercial Distribution

  • 10840642140002 ()
11-7411

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, O-U, Double, Small
Spine Wave, Inc.
11-7410
In Commercial Distribution

  • 10840642139990 ()
11-7410

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, O-U, Large
Spine Wave, Inc.
11-7409
In Commercial Distribution

  • 10840642139983 ()
11-7409

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, O-U, Medium
Spine Wave, Inc.
11-7408
In Commercial Distribution

  • 10840642139976 ()
11-7408

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, O-U, Small
Spine Wave, Inc.
11-7407
In Commercial Distribution

  • 10840642139969 ()
11-7407

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, C-C, Double, Large
Spine Wave, Inc.
11-7406
In Commercial Distribution

  • 10840642139952 ()
11-7406

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, C-C, Double, Medium
Spine Wave, Inc.
11-7405
In Commercial Distribution

  • 10840642139945 ()
11-7405

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, C-C, Double, Small
Spine Wave, Inc.
11-7404
In Commercial Distribution

  • 10840642139938 ()
11-7404

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, C-C, Large
Spine Wave, Inc.
11-7403
In Commercial Distribution

  • 10840642139921 ()
11-7403

  • Bone-screw internal spinal fixation system connector
Connector, Parallel, C-C, Medium
Spine Wave, Inc.
11-7402
In Commercial Distribution

  • 10840642139914 ()
11-7402

  • Bone-screw internal spinal fixation system connector
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