SEARCH RESULTS FOR: (*purchase New Brunswick driver*)(15741 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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Indy - 00843210137759

34mm x 26mm, 8°, 17mm PEEK Spacer
Altus Spine, LLC
FA34260817
In Commercial Distribution

  • 00843210137759 ()


  • Spinal implant trial

Indy - 00843210137742

34mm x 26mm, 8°, 15mm PEEK Spacer
Altus Spine, LLC
FA34260815
In Commercial Distribution

  • 00843210137742 ()


  • Spinal implant trial

Indy - 00843210137735

34mm x 26mm, 8°, 13mm PEEK Spacer
Altus Spine, LLC
FA34260813
In Commercial Distribution

  • 00843210137735 ()


  • Spinal implant trial

Indy - 00843210137728

34mm x 26mm, 8°, 11mm PEEK Spacer
Altus Spine, LLC
FA34260811
In Commercial Distribution

  • 00843210137728 ()


  • Spinal implant trial

Indy - 00843210137711

34mm x 26mm, 8°, 9mm PEEK Spacer
Altus Spine, LLC
FA34260809
In Commercial Distribution

  • 00843210137711 ()


  • Spinal implant trial

Indy - 00843210137704

32mm x 24mm, 25°, 19mm PEEK Spacer
Altus Spine, LLC
FA32242519
In Commercial Distribution

  • 00843210137704 ()


  • Spinal implant trial

Indy - 00843210137698

32mm x 24mm, 25°, 17mm PEEK Spacer
Altus Spine, LLC
FA32242517
In Commercial Distribution

  • 00843210137698 ()


  • Spinal implant trial

Indy - 00843210137681

32mm x 24mm, 25°, 15mm PEEK Spacer
Altus Spine, LLC
FA32242515
In Commercial Distribution

  • 00843210137681 ()


  • Spinal implant trial

Indy - 00843210137674

32mm x 24mm, 20°, 19mm PEEK Spacer
Altus Spine, LLC
FA32242019
In Commercial Distribution

  • 00843210137674 ()


  • Spinal implant trial

Indy - 00843210137667

32mm x 24mm, 20°, 17mm PEEK Spacer
Altus Spine, LLC
FA32242017
In Commercial Distribution

  • 00843210137667 ()


  • Spinal implant trial
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