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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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GRANULES 60000010INT PLEXUR P 10CC
MEDTRONIC SOFAMOR DANEK, INC.
60000010INT
In Commercial Distribution

  • 00643169218277 ()

  • 10cc


  • Bone matrix implant, human-derived
GRANULES 60000020INT PLEXUR P 20 CC
MEDTRONIC SOFAMOR DANEK, INC.
60000020INT
In Commercial Distribution

  • 00643169218253 ()

  • 20cc


  • Bone matrix implant, human-derived
GRANULES 60000030INT PLEXUR P 30 CC
MEDTRONIC SOFAMOR DANEK, INC.
60000030INT
In Commercial Distribution

  • 00643169218239 ()

  • 30cc


  • Bone matrix implant, human-derived
WEDGE 60000215INT PLEXUR P 40MMX15MMX15
MEDTRONIC SOFAMOR DANEK, INC.
60000215INT
In Commercial Distribution

  • 00643169218130 ()

  • 40mm x 15mm x 15DEG


  • Bone matrix implant, human-derived
BLCK 60000310INT PLEXUR P 10MMX10MMX20MM
MEDTRONIC SOFAMOR DANEK, INC.
60000310INT
In Commercial Distribution

  • 00643169218116 ()

  • 10mm x 10mm x 20mm


  • Bone matrix implant, human-derived
BLCK 60000320INT PLEXUR P 20MMX20MMX20MM
MEDTRONIC SOFAMOR DANEK, INC.
60000320INT
In Commercial Distribution

  • 00643169218093 ()

  • 20mm x 20mm x 20mm


  • Bone matrix implant, human-derived
DBM 7509510 MAGNIFUSE II 2.5 CM X 10 CM
MEDTRONIC SOFAMOR DANEK, INC.
7509510
In Commercial Distribution

  • 00643169216242 ()

  • 2.5cm x 10cm


  • Bone matrix implant, human-derived
DBM 7509505 MAGNIFUSE II 2.5 CM X 5 CM
MEDTRONIC SOFAMOR DANEK, INC.
7509505
In Commercial Distribution

  • 00643169216235 ()

  • 2.5cm X 5cm


  • Bone matrix implant, human-derived
BONE GRAFT 7509141INT MG 1.75 CM X 10 CM
MEDTRONIC SOFAMOR DANEK, INC.
7509141INT
In Commercial Distribution

  • 00643169141858 ()

  • 1.75cm x 10cm


  • Bone matrix implant, human-derived
No Description
Hans Biomed Corp.
FG100
In Commercial Distribution

  • 08809204339945 ()


  • Bone matrix implant, human-derived
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