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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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Allograft Paste IC 5cc
Rti Surgical, Inc.
802205
In Commercial Distribution

  • 00898623002088 ()


  • Bone matrix implant, human-derived
Allograft Paste IC, RT, 3cc
Rti Surgical, Inc.
802203
In Commercial Distribution

  • 00898623002071 ()


  • Bone matrix implant, human-derived
Allograft Paste IC, RT, 2cc
Rti Surgical, Inc.
802202
In Commercial Distribution

  • 00898623002064 ()


  • Bone matrix implant, human-derived
Allograft Paste IC, RT, 1cc
Rti Surgical, Inc.
802201
In Commercial Distribution

  • 00898623002057 ()


  • Bone matrix implant, human-derived
Allograft Paste IC 10cc
Rti Surgical, Inc.
802110
In Commercial Distribution

  • 00898623002040 ()


  • Bone matrix implant, human-derived
Allograft Paste IC 5cc
Rti Surgical, Inc.
802105
In Commercial Distribution

  • 00898623002033 ()


  • Bone matrix implant, human-derived
Allograft Paste 10cc
Rti Surgical, Inc.
801210
In Commercial Distribution

  • 00898623002026 ()


  • Bone matrix implant, human-derived
Allograft Paste 5cc
Rti Surgical, Inc.
801205
In Commercial Distribution

  • 00898623002019 ()


  • Bone matrix implant, human-derived
Allograft Paste 1cc
Rti Surgical, Inc.
801201
In Commercial Distribution

  • 00898623002002 ()


  • Bone matrix implant, human-derived
The Tinnitus custom device utilizes advanced digital signal processing with broadband white or pink noise integrated into a cosmetically appealing design. Designed for patients that suffer from Tinnitus to ease ringing in the ear.
GENERAL HEARING INSTRUMENT, INC.
Tinnitus,Custom,Pair
In Commercial Distribution

  • 00089518000801 ()


  • Air-conduction tinnitus masker, in-the-ear
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