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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
FGX INTERNATIONAL INC.
ARD302-125.MCV
In Commercial Distribution

  • 00193033595404 ()


  • Prescription spectacles
Interbody, 9mm x 24mm x 16mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WO1-924165
In Commercial Distribution

  • 10889981234928 ()
WO1-924165

  • Metallic spinal interbody fusion cage
Interbody, 9mm x 24mm x 14mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WO1-924145
In Commercial Distribution

  • 10889981234843 ()
WO1-924145

  • Metallic spinal interbody fusion cage
Interbody, 9mm x 24mm x 12mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WO1-924125
In Commercial Distribution

  • 10889981234768 ()
WO1-924125

  • Metallic spinal interbody fusion cage
Interbody, 9mm x 24mm x 10mm, 15 Deg, 3D
Seaspine Orthopedics Corporation
WO1-924105
In Commercial Distribution

  • 10889981234683 ()
WO1-924105

  • Metallic spinal interbody fusion cage
No Description
Biomet Orthopedics, LLC
478735
In Commercial Distribution

  • 00880304386952 ()
478735

  • Orthopaedic implant-instrument extension adaptor, reusable
No Description
FGX INTERNATIONAL INC.
3865003.LTS
Not in Commercial Distribution

  • 00999999005977 ()


  • Prescription spectacles
No Description
FGX INTERNATIONAL INC.
DL4048/28.SDM
In Commercial Distribution

  • 00057800939993 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
DL4046/4.SDM
In Commercial Distribution

  • 00057800939979 ()


  • Tinted non-prescription spectacles
No Description
FGX INTERNATIONAL INC.
DL4050/8.SDM
In Commercial Distribution

  • 00057800940401 ()


  • Tinted non-prescription spectacles
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