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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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Zimmer, Inc.
00-8754-004-28
In Commercial Distribution

  • 00889024150355 ()

  • Size CC
  • Lumen/Inner Diameter: 28 Millimeter
00-8754-004-28

  • Non-constrained polyethylene acetabular liner
STIMUBLAST® CB DBM Paste, 8cc
ALLOSOURCE
ABS-2004-08
In Commercial Distribution

  • M536ABS2004081 ()

  • 8 cc
ABS-2004-08

  • Bone matrix implant, human-derived
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
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