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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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BioSet® - 00854095006443

DBM Paste
Rti Surgical, Inc.
007845
In Commercial Distribution

  • 00854095006443 ()
007845

  • Bone matrix implant, human-derived

BioSet® - 00854095006436

DBM Paste
Rti Surgical, Inc.
007830
In Commercial Distribution

  • 00854095006436 ()
007830

  • Bone matrix implant, human-derived

BioSet® - 00854095006429

DBM Paste
Rti Surgical, Inc.
007820
In Commercial Distribution

  • 00854095006429 ()
007820

  • Bone matrix implant, human-derived

BioSet® - 00854095006412

DBM Paste
Rti Surgical, Inc.
006820
In Commercial Distribution

  • 00854095006412 ()
006820

  • Bone matrix implant, human-derived

BioSet® - 00854095006405

DBM Paste
Rti Surgical, Inc.
006810
In Commercial Distribution

  • 00854095006405 ()
006810

  • Bone matrix implant, human-derived

BioSet® - 00854095006399

DBM Paste
Rti Surgical, Inc.
006805
In Commercial Distribution

  • 00854095006399 ()
006805

  • Bone matrix implant, human-derived

BioSet® - 00854095006344

DBM Paste
Rti Surgical, Inc.
005810
In Commercial Distribution

  • 00854095006344 ()
005810

  • Bone matrix implant, human-derived

BioSet® - 00854095006337

DBM Paste
Rti Surgical, Inc.
005805
In Commercial Distribution

  • 00854095006337 ()
005805

  • Bone matrix implant, human-derived

BioSet® - 00854095006320

DBM Paste
Rti Surgical, Inc.
005801
In Commercial Distribution

  • 00854095006320 ()
005801

  • Bone matrix implant, human-derived

BioSet® - 00854095006313

DBM Paste
Rti Surgical, Inc.
005800
In Commercial Distribution

  • 00854095006313 ()
005800

  • Bone matrix implant, human-derived
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