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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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STIMUBLAST® CB DBM Paste, 3cc
ALLOSOURCE
ABS-2004-03
In Commercial Distribution

  • M536ABS2004031 ()

  • 3 cc
ABS-2004-03

  • Bone matrix implant, human-derived
STIMUBLAST® CB DBM Paste, 1cc
ALLOSOURCE
ABS-2004-01
In Commercial Distribution

  • M536ABS2004011 ()

  • 1 cc
ABS-2004-01

  • Bone matrix implant, human-derived
STIMUBLAST® CB DBM Putty, 10cc
ALLOSOURCE
ABS-2003-10
In Commercial Distribution

  • M536ABS2003101 ()

  • 10 cc
ABS-2003-10

  • Bone matrix implant, human-derived
STIMUBLAST® CB DBM Putty, 5cc
ALLOSOURCE
ABS-2003-05
In Commercial Distribution

  • M536ABS2003051 ()

  • 5 cc
ABS-2003-05

  • Bone matrix implant, human-derived
STIMUBLAST® DBM Gel, 10cc
ALLOSOURCE
ABS-2002-10
In Commercial Distribution

  • M536ABS2002101 ()

  • 10 cc
ABS-2002-10

  • Bone matrix implant, human-derived
STIMUBLAST® DBM Gel, 5cc
ALLOSOURCE
ABS-2002-05
In Commercial Distribution

  • M536ABS2002051 ()

  • 5 cc
ABS-2002-05

  • Bone matrix implant, human-derived
STIMUBLAST® DBM Gel, 1cc
ALLOSOURCE
ABS-2002-01
In Commercial Distribution

  • M536ABS2002011 ()

  • 1 cc
ABS-2002-01

  • Bone matrix implant, human-derived
STIMUBLAST® DBM Putty, 5cc
ALLOSOURCE
ABS-2001-05
In Commercial Distribution

  • M536ABS2001051 ()

  • 5 cc
ABS-2001-05

  • Bone matrix implant, human-derived
STIMUBLAST® DBM Putty, 1cc
ALLOSOURCE
ABS-2001-01
In Commercial Distribution

  • M536ABS2001011 ()

  • 1 cc
ABS-2001-01

  • Bone matrix implant, human-derived
AlloFuse® Plus DBM Putty, 5cc
ALLOSOURCE
90338005
In Commercial Distribution

  • M536903380051 ()

  • 5 cc
90338005

  • Bone matrix implant, human-derived
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