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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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Tinnitus app Android version 1.0
Widex A/S
Tinnitus app
In Commercial Distribution

  • 05706069674729 ()
5 300 0007 001

  • Tinnitus masking application software
Tinnitus app iOS version 1.0
Widex A/S
Tinnitus app
In Commercial Distribution

  • 05706069674712 ()
5 300 0006 001

  • Tinnitus masking application software
No Description
PIVOTAL HEALTH SOLUTIONS, INC.
ET109
In Commercial Distribution

  • 00850020142279 ()


  • Examination/treatment table, manual
No Description
PIVOTAL HEALTH SOLUTIONS, INC.
ET108
In Commercial Distribution

  • 00850020142262 ()


  • Examination/treatment table, manual
No Description
PIVOTAL HEALTH SOLUTIONS, INC.
ET107
In Commercial Distribution

  • 00850020142255 ()


  • Examination/treatment table, manual
No Description
PIVOTAL HEALTH SOLUTIONS, INC.
ET106
In Commercial Distribution

  • 00850020142248 ()


  • Examination/treatment table, manual
Non-electric, fixed height model in the ET series of treatment cabinets with an open shelf.
PIVOTAL HEALTH SOLUTIONS, INC.
ET105
In Commercial Distribution

  • 00850020142231 ()


  • Examination/treatment table, manual
DEMINERALIZED BONE MATRIX (DMB) 0.5CC
BIOMET 3I, LLC
ROAP05
In Commercial Distribution

  • 00844868035497 ()

  • Volume 0.5 mL


  • Dental bone matrix implant, human-derived
DEMINERALIZED BONE MATRIX (DMB) 2.0CC
BIOMET 3I, LLC
ROAP20
In Commercial Distribution

  • 00844868035510 ()

  • Volume 2 mL


  • Dental bone matrix implant, human-derived
DEMINERALIZED BONE MATRIX (DMB) 1.0CC
BIOMET 3I, LLC
ROAP10
In Commercial Distribution

  • 00844868035503 ()

  • Volume 1 mL


  • Dental bone matrix implant, human-derived
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