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

  • M536902380081 ()

  • 8 cc
90238008

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 10cc
ALLOSOURCE
90138010
In Commercial Distribution

  • M536901380101 ()

  • 10 cc
90138010

  • Bone matrix implant, human-derived
No Description
Zimmer, Inc.
00-8852-004-22
In Commercial Distribution

  • 00889024364486 ()

  • Lumen/Inner Diameter: 22 Millimeter
  • Size CC
00-8852-004-22

  • Non-constrained polyethylene acetabular liner
No Description
Zimmer, Inc.
00-8753-040-02
In Commercial Distribution

  • 00889024364400 ()

  • Size CC
  • Outer Diameter: 40 Millimeter
00-8753-040-02

  • Acetabular shell
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