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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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Mediastinal Drain, Silicone, Eyes On Top & Bottom, With ClotStop®
AXIOM MEDICAL, INCORPORATED
111059AT
In Commercial Distribution

  • M665111059AT3 ()
  • M665111059AT1 ()
  • M665111059AT0 ()

  • 5 mm


  • Mediastinal drainage catheter, non-antimicrobial
Mediastinal Drain, Silicone, Eyes On Top & Bottom
AXIOM MEDICAL, INCORPORATED
111059
In Commercial Distribution

  • M6651110593 ()
  • M6651110591 ()
  • M6651110590 ()

  • 5 mm


  • Mediastinal drainage catheter, non-antimicrobial
Phosphocalcic ceramic
KASIOS
K43105G
In Commercial Distribution

  • M505K43105G0 ()

  • 5 cm³


  • Synthetic bone graft
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, 5cc
ALLOSOURCE
ABS-2002-05
In Commercial Distribution

  • M536ABS2002051 ()

  • 5 cc
ABS-2002-05

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

  • M536903380051 ()

  • 5 cc
90338005

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 5 cc
ALLOSOURCE
90138005
In Commercial Distribution

  • M536901380051 ()

  • 5 cc
90138005

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 5 cc
ALLOSOURCE
90038005
In Commercial Distribution

  • M536900380051 ()

  • 5 cc
90038005

  • Bone matrix implant, human-derived
IDENTITY IMPRINT POROUS CR FEMORAL IMPLANT SIZE 5 LEFT OR RIGHT
Conformis, Inc.
TCR-102-F05S-01
In Commercial Distribution

  • M572TCR102F05S011 ()

  • size 5
TCR-102-F05S

  • Cruciate-retaining total knee prosthesis
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