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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
IMPLANT DIRECT SYBRON MANUFACTURING LLC
1000-08
Not in Commercial Distribution

  • 10841307108658 ()
  • 00841307108651 ()
1000-08

  • Dental implant suprastructure, permanent, preformed
No Description
IMPLANT DIRECT SYBRON MANUFACTURING LLC
1000-06
In Commercial Distribution

  • 10841307108641 ()
  • 00841307108644 ()
1000-06

  • Dental implant suprastructure, permanent, preformed
BAG,2 LITER,NON-LATEX
PARKER-HANNIFIN CORPORATION
4100-2NL
In Commercial Distribution

  • 00816711020868 ()
4100-2NL

  • Breathing circuit bag, reusable
Spinous process compression forceps
SpineArt SA
PAD-IN 12 00-N
In Commercial Distribution

  • 07640178975040 ()
PAD-IN 12 00-N

  • Bone distraction forceps
Multiaxial Plate Inserter
SpineArt SA
PAD-IN 11 00-N
In Commercial Distribution

  • 07640178972155 ()
PAD-IN 11 00-N

  • Surgical implant/trial-implant/sizer holder, reusable
Locking Plate Inserter
SpineArt SA
PAD-IN 10 00-N
In Commercial Distribution

  • 07640178972148 ()
PAD-IN 10 00-N

  • Surgical implant/trial-implant/sizer holder, reusable
Compression forceps
SpineArt SA
SPE-IN 00 72-N
In Commercial Distribution

  • 07640178973756 ()
SPE-IN 00 72-N

  • Bone distraction forceps
Plate template 3 level 72mm
SpineArt SA
TRY-IN 08 72-N
In Commercial Distribution

  • 07640178983441 ()
TRY-IN 08 72-N

  • Spinal implant trial
Plate template 3 level 68mm
SpineArt SA
TRY-IN 08 68-N
In Commercial Distribution

  • 07640178983434 ()
TRY-IN 08 68-N

  • Spinal implant trial
Plate template 3 level 61mm
SpineArt SA
TRY-IN 08 61-N
In Commercial Distribution

  • 07640178983410 ()
TRY-IN 08 61-N

  • Spinal implant trial
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