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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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No Description
Biomet Orthopedics, LLC
184201
In Commercial Distribution

  • 00880304435520 ()

  • 10 MM 57.5 MM
184201

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184290
In Commercial Distribution

  • 00880304435490 ()

  • 15 MM 80 MM
184290

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184262
In Commercial Distribution

  • 00880304435469 ()

  • 15 MM 60 MM
184262

  • Knee arthroplasty wedge
OsteoStrux® Strip, 10cc
Seaspine Orthopedics Corporation
56010100ITL
In Commercial Distribution

  • 10889981123369 ()

  • 10cc
56010100ITL

  • Bone matrix implant, composite
No Description
Biomet Orthopedics, LLC
184266
In Commercial Distribution

  • 00880304435445 ()

  • 15 MM 70 MM
184266

  • Knee arthroplasty wedge
OsteoStrux® Putty, 5cc
Seaspine Orthopedics Corporation
56070050ITL
In Commercial Distribution

  • 10889981123338 ()

  • 5cc
56070050ITL

  • Bone matrix implant, composite
No Description
Biomet Orthopedics, LLC
184246
In Commercial Distribution

  • 00880304435421 ()

  • 10 MM 70 MM
184246

  • Knee arthroplasty wedge
IsoTis Mozaik™ Strip, 15cc
Seaspine Orthopedics Corporation
CCM10256ITL
In Commercial Distribution

  • 10889981123314 ()

  • 15cc
CCM10256ITL

  • Bone matrix implant, composite
IsoTis Mozaik™ Strip, 10cc
Seaspine Orthopedics Corporation
CCM10210ITL
In Commercial Distribution

  • 10889981123307 ()

  • 10cc
CCM10210ITL

  • Bone matrix implant, composite
IsoTis Mozaik™ Putty, 15cc
Seaspine Orthopedics Corporation
PTY10256ITL
In Commercial Distribution

  • 10889981123291 ()

  • 15cc
PTY10256ITL

  • Bone matrix implant, composite
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