SEARCH RESULTS FOR: (*fake 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 - 00843210137605

32mm x 24mm, 16°, 13mm PEEK Spacer
Altus Spine, LLC
FA32241613
In Commercial Distribution

  • 00843210137605 ()


  • Spinal implant trial

Indy - 00843210137599

32mm x 24mm, 16°, 11mm PEEK Spacer
Altus Spine, LLC
FA32241611
In Commercial Distribution

  • 00843210137599 ()


  • Spinal implant trial

Indy - 00843210137582

32mm x 24mm, 12°, 19mm PEEK Spacer
Altus Spine, LLC
FA32241219
In Commercial Distribution

  • 00843210137582 ()


  • Spinal implant trial

Indy - 00843210137575

32mm x 24mm, 12°, 17mm PEEK Spacer
Altus Spine, LLC
FA32241217
In Commercial Distribution

  • 00843210137575 ()


  • Spinal implant trial

Indy - 00843210137551

32mm x 24mm, 12°, 15mm PEEK Spacer
Altus Spine, LLC
FA32241215
In Commercial Distribution

  • 00843210137551 ()


  • Spinal implant trial

Indy - 00843210137544

32mm x 24mm, 12°, 13mm PEEK Spacer
Altus Spine, LLC
FA32241213
In Commercial Distribution

  • 00843210137544 ()


  • Spinal implant trial

Indy - 00843210137537

32mm x 24mm, 12°, 11mm PEEK Spacer
Altus Spine, LLC
FA32241211
In Commercial Distribution

  • 00843210137537 ()


  • Spinal implant trial

Indy - 00843210137520

32mm x 24mm, 12°, 9mm PEEK Spacer
Altus Spine, LLC
FA32241209
In Commercial Distribution

  • 00843210137520 ()


  • Spinal implant trial

Indy - 00843210137513

32mm x 24mm, 8°, 19mm PEEK Spacer
Altus Spine, LLC
FA32240819
In Commercial Distribution

  • 00843210137513 ()


  • Spinal implant trial

Indy - 00843210137506

32mm x 24mm, 8°, 17mm PEEK Spacer
Altus Spine, LLC
FA32240817
In Commercial Distribution

  • 00843210137506 ()


  • Spinal implant trial
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