SEARCH RESULTS FOR: (*d47 external mil*)(162601 results)

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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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Premiere Posterior Night Splint, Large
Elite Orthopaedics, Inc.
T58126
In Commercial Distribution

  • 00816591011741 ()
T58126

  • Ankle/foot orthosis
Premiere Posterior Night Splint, Medium
Elite Orthopaedics, Inc.
T58124
In Commercial Distribution

  • 00816591011734 ()
T58124

  • Ankle/foot orthosis
Premiere Posterior Night Splint, Small
Elite Orthopaedics, Inc.
T58122
In Commercial Distribution

  • 00816591011727 ()
T58122

  • Ankle/foot orthosis
Premiere Pneumatic Fracture Walker, Low, X-Large
Elite Orthopaedics, Inc.
T12128
In Commercial Distribution

  • 00816591011697 ()
T12128

  • Ankle/foot orthosis
Premiere Pneumatic Fracture Walker, Low, Large
Elite Orthopaedics, Inc.
T12126
In Commercial Distribution

  • 00816591011680 ()
T12126

  • Ankle/foot orthosis
Premiere Pneumatic Fracture Walker, Low, Medium
Elite Orthopaedics, Inc.
T12124
In Commercial Distribution

  • 00816591011673 ()
T12124

  • Ankle/foot orthosis
Premiere Pneumatic Fracture Walker, Low, Small
Elite Orthopaedics, Inc.
T12122
In Commercial Distribution

  • 00816591011666 ()
T12122

  • Ankle/foot orthosis
Premiere Pneumatic Fracture Walker, High, X-Large
Elite Orthopaedics, Inc.
T12028
In Commercial Distribution

  • 00816591011659 ()
T12028

  • Ankle/foot orthosis
Premiere Pneumatic Fracture Walker, High, Large
Elite Orthopaedics, Inc.
T12026
In Commercial Distribution

  • 00816591011642 ()
T12026

  • Ankle/foot orthosis
Premiere Pneumatic Fracture Walker, High, Medium
Elite Orthopaedics, Inc.
T12024
In Commercial Distribution

  • 00816591011635 ()
T12024

  • Ankle/foot orthosis
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