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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® - M536ABS2003051

STIMUBLAST® CB DBM Putty, 5cc
ALLOSOURCE
ABS-2003-05
In Commercial Distribution

  • M536ABS2003051 ()

  • 5 cc
ABS-2003-05

  • Bone matrix implant, human-derived

STIMUBLAST® - M536ABS2002101

STIMUBLAST® DBM Gel, 10cc
ALLOSOURCE
ABS-2002-10
In Commercial Distribution

  • M536ABS2002101 ()

  • 10 cc
ABS-2002-10

  • Bone matrix implant, human-derived

STIMUBLAST® - M536ABS2002051

STIMUBLAST® DBM Gel, 5cc
ALLOSOURCE
ABS-2002-05
In Commercial Distribution

  • M536ABS2002051 ()

  • 5 cc
ABS-2002-05

  • Bone matrix implant, human-derived

STIMUBLAST® - M536ABS2002011

STIMUBLAST® DBM Gel, 1cc
ALLOSOURCE
ABS-2002-01
In Commercial Distribution

  • M536ABS2002011 ()

  • 1 cc
ABS-2002-01

  • Bone matrix implant, human-derived

STIMUBLAST® - M536ABS2001051

STIMUBLAST® DBM Putty, 5cc
ALLOSOURCE
ABS-2001-05
In Commercial Distribution

  • M536ABS2001051 ()

  • 5 cc
ABS-2001-05

  • Bone matrix implant, human-derived

STIMUBLAST® - M536ABS2001011

STIMUBLAST® DBM Putty, 1cc
ALLOSOURCE
ABS-2001-01
In Commercial Distribution

  • M536ABS2001011 ()

  • 1 cc
ABS-2001-01

  • Bone matrix implant, human-derived

AlloFuse® Plus - M536903380051

AlloFuse® Plus DBM Putty, 5cc
ALLOSOURCE
90338005
In Commercial Distribution

  • M536903380051 ()

  • 5 cc
90338005

  • Bone matrix implant, human-derived

AlloFuse® Plus - M536902380081

AlloFuse® Plus DBM Paste, 8cc
ALLOSOURCE
90238008
In Commercial Distribution

  • M536902380081 ()

  • 8 cc
90238008

  • Bone matrix implant, human-derived

AlloFuse® - M536901380101

AlloFuse® DBM Gel, 10cc
ALLOSOURCE
90138010
In Commercial Distribution

  • M536901380101 ()

  • 10 cc
90138010

  • Bone matrix implant, human-derived

Collage Osteoconductive Scaffold - Putty - 10381780114352

The Orthofix Collage Osteoconductive Scaffold - Putty (Orthofix Collage Putty) is a resorbable bone void filler made from a porous highly purified collagen matrix that has high purity tricalcium phosphate (TCP) granules dispersed throughout. The implant is provided sterile, nonpyrogenic, for single use in double peel packages. The Orthofix Collage Putty bone grafting construct is designed to facilitate the repair of bony defects. In the dry state, the matrix has a three dimensional trabecular network of pores that resembles the pore structure of human cancellous bone. The Orthofix Collage Putty quickly imbibes fluids, making it easy to combine with bone marrow aspirate. The Orthofix Collage Putty guides the regeneration of bone across the defect site into which the Putty is implanted. New bone forms in apposition to the matrix surface when the graft is placed in direct contact with viable host bone. Ultimately the matrix is resorbed and remodeled into bone.
Integra Lifesciences Corporation
710015
Not in Commercial Distribution

  • M2697100151 ()
  • 10381780114352 ()

  • 15 cc
710015

  • Bone matrix implant, composite
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