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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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APEX Deformity Instruments Case
SPINECRAFT, LLC
6000-200B
In Commercial Distribution

  • 00193082079382 ()
6000-200B

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 12 x 28mm
SPINECRAFT, LLC
1032-12-028
In Commercial Distribution

  • 00193082079337 ()
1032-12-028

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 12 x 26mm
SPINECRAFT, LLC
1032-12-026
In Commercial Distribution

  • 00193082079320 ()
1032-12-026

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 11 x 28mm
SPINECRAFT, LLC
1032-11-028
In Commercial Distribution

  • 00193082079313 ()
1032-11-028

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 11 x 26mm
SPINECRAFT, LLC
1032-11-026
In Commercial Distribution

  • 00193082079306 ()
1032-11-026

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 10 x 28mm
SPINECRAFT, LLC
1032-10-028
In Commercial Distribution

  • 00193082079290 ()
1032-10-028

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 10 x 26mm
SPINECRAFT, LLC
1032-10-026
In Commercial Distribution

  • 00193082079283 ()
1032-10-026

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 9 x 28mm
SPINECRAFT, LLC
1032-09-028
In Commercial Distribution

  • 00193082079276 ()
1032-09-028

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 9 x 26mm
SPINECRAFT, LLC
1032-09-026
In Commercial Distribution

  • 00193082079269 ()
1032-09-026

  • General internal orthopaedic fixation system implantation kit
MIS Straight TLIF Trial, 8 x 28mm
SPINECRAFT, LLC
1032-08-028
In Commercial Distribution

  • 00193082079252 ()
1032-08-028

  • General internal orthopaedic fixation system implantation kit
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