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 - 00843210138350

32mm x 24mm, 8°, 9mm Ti Spacer
Altus Spine, LLC
FA32240809T
In Commercial Distribution

  • 00843210138350 ()


  • Spinal implant trial

Indy - 00843210138343

42mm x 30mm, 25°, 19mm PEEK Spacer
Altus Spine, LLC
FA42302519
In Commercial Distribution

  • 00843210138343 ()


  • Spinal implant trial

Indy - 00843210138336

42mm x 30mm, 25°, 17mm PEEK Spacer
Altus Spine, LLC
FA42302517
In Commercial Distribution

  • 00843210138336 ()


  • Spinal implant trial

Indy - 00843210138329

42mm x 30mm, 20°, 19mm PEEK Spacer
Altus Spine, LLC
FA42302019
In Commercial Distribution

  • 00843210138329 ()


  • Spinal implant trial

Indy - 00843210138312

42mm x 30mm, 20°, 17mm PEEK Spacer
Altus Spine, LLC
FA42302017
In Commercial Distribution

  • 00843210138312 ()


  • Spinal implant trial

Indy - 00843210138305

42mm x 30mm, 20°, 15mm PEEK Spacer
Altus Spine, LLC
FA42302015
In Commercial Distribution

  • 00843210138305 ()


  • Spinal implant trial

Indy - 00843210138299

42mm x 30mm, 16°, 19mm PEEK Spacer
Altus Spine, LLC
FA42301619
In Commercial Distribution

  • 00843210138299 ()


  • Spinal implant trial

Indy - 00843210138282

42mm x 30mm, 16°, 17mm PEEK Spacer
Altus Spine, LLC
FA42301617
In Commercial Distribution

  • 00843210138282 ()


  • Spinal implant trial

Indy - 00843210138275

42mm x 30mm, 16°, 15mm PEEK Spacer
Altus Spine, LLC
FA42301615
In Commercial Distribution

  • 00843210138275 ()


  • Spinal implant trial

Indy - 00843210138268

42mm x 30mm, 16°, 13mm PEEK Spacer
Altus Spine, LLC
FA42301613
In Commercial Distribution

  • 00843210138268 ()


  • Spinal implant trial
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