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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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SA ALIF Trial, 27Dx36Wx12H, 20°
NEXXT SPINE, LLC
I61-TR2736-12-20
In Commercial Distribution

  • 00889929043561 ()


  • General internal orthopaedic fixation system implantation kit
SA ALIF Trial, 24Dx32Wx20H, 20°
NEXXT SPINE, LLC
I61-TR2432-20-20
In Commercial Distribution

  • 00889929043400 ()


  • General internal orthopaedic fixation system implantation kit
SA ALIF Trial, 24Dx32Wx18H, 20°
NEXXT SPINE, LLC
I61-TR2432-18-20
In Commercial Distribution

  • 00889929043394 ()


  • General internal orthopaedic fixation system implantation kit
SA ALIF Trial, 24Dx32Wx16H, 20°
NEXXT SPINE, LLC
I61-TR2432-16-20
In Commercial Distribution

  • 00889929043387 ()


  • General internal orthopaedic fixation system implantation kit
SA ALIF Trial, 24Dx32Wx14H, 20°
NEXXT SPINE, LLC
I61-TR2432-14-20
In Commercial Distribution

  • 00889929043370 ()


  • General internal orthopaedic fixation system implantation kit
SA ALIF Trial, 24Dx32Wx12H, 20°
NEXXT SPINE, LLC
I61-TR2432-12-20
In Commercial Distribution

  • 00889929043363 ()


  • General internal orthopaedic fixation system implantation kit
Met-Cuneiform Guide, Left, 20°/28°
Paragon 28, Inc.
P30-942-L120
In Commercial Distribution

  • 00889795049711 ()
P30-942-L120

  • Osteotomy guide, reusable
Met-Cuneiform Guide, Right, 20°/28°
Paragon 28, Inc.
P30-942-R120
In Commercial Distribution

  • 00889795049704 ()
P30-942-R120

  • Osteotomy guide, reusable
Met-Cuneiform Guide, Left, 12°/20°
Paragon 28, Inc.
P30-942-L112
In Commercial Distribution

  • 00889795049636 ()
P30-942-L112

  • Osteotomy guide, reusable
Met-Cuneiform Guide, Right, 12°/20°
Paragon 28, Inc.
P30-942-R112
In Commercial Distribution

  • 00889795049629 ()
P30-942-R112

  • Osteotomy guide, reusable
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