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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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Cage, 21x12mm, 8° TA
Kalitec Direct LLC
12-PCT-2112
In Commercial Distribution

  • B07312PCT21120 ()


  • Polymeric spinal interbody fusion cage
Cage, 21x11mm, 8° TA
Kalitec Direct LLC
12-PCT-2111
In Commercial Distribution

  • B07312PCT21110 ()


  • Polymeric spinal interbody fusion cage
Cage, 21x10mm, 8° TA
Kalitec Direct LLC
12-PCT-2110
In Commercial Distribution

  • B07312PCT21100 ()


  • Polymeric spinal interbody fusion cage
Cage, 21x9mm, 8° TA
Kalitec Direct LLC
12-PCT-2109
In Commercial Distribution

  • B07312PCT21090 ()


  • Polymeric spinal interbody fusion cage
Cage, 21x8mm, 8° TA
Kalitec Direct LLC
12-PCT-2108
In Commercial Distribution

  • B07312PCT21080 ()


  • Polymeric spinal interbody fusion cage
29x39x13, 8°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L138
In Commercial Distribution

  • B0621750L138 ()
1750-L138

  • Surgical instrument/implant depth limiter, reusable
29x39x11, 8°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L118
In Commercial Distribution

  • B0621750L118 ()
1750-L118

  • Surgical instrument/implant depth limiter, reusable
29x39x09, 8°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L098
In Commercial Distribution

  • B0621750L098 ()
1750-L098

  • Surgical instrument/implant depth limiter, reusable
29x39x07, 8°, Trial, PISCES-SA
Osseus Fusion Systems, LLC
1750-L078
In Commercial Distribution

  • B0621750L078 ()
1750-L078

  • Surgical instrument/implant depth limiter, reusable
20x55x8, 8 degree, LLIF
Osseus Fusion Systems, LLC
1400-1230
In Commercial Distribution

  • B06214001230 ()
1400-1230S

  • Metallic spinal interbody fusion cage
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