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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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TAP Ø 4.5 X 30
SpineArt SA
SPE-IN 01 36-N
In Commercial Distribution

  • 07640178980129 ()
SPE-IN 01 36-N

  • Bone tap, reusable
TAP Ø 6.5 X 30
SpineArt SA
SPE-IN 01 38-N
In Commercial Distribution

  • 07640178980112 ()
SPE-IN 01 38-N

  • Bone tap, reusable
TAP Ø 5.5 X 30
SpineArt SA
SPE-IN 01 37-N
In Commercial Distribution

  • 07640178980105 ()
SPE-IN 01 37-N

  • Bone tap, reusable
4.0 TIGHTENER
SpineArt SA
SPE-IN 00 90-N
In Commercial Distribution

  • 07640178979901 ()
SPE-IN 00 90-N

  • Surgical screwdriver, reusable
Setcrew holder
SpineArt SA
ELL-IN 04 10-N
Not in Commercial Distribution

  • 07640151093860 ()
ELL-IN 04 10-N

  • General internal orthopaedic fixation system implantation kit
Setcrew driver
SpineArt SA
ELL-IN 07 06-N
Not in Commercial Distribution

  • 07640151093846 ()
ELL-IN 07 06-N

  • General internal orthopaedic fixation system implantation kit
CLIPPING TUBE OPEN
SpineArt SA
MIS-IN 19 04-N
In Commercial Distribution

  • 07640151089580 ()
MIS-IN 19 04-N

  • Orthopaedic implantation sleeve, reusable
TAB BREAKER
SpineArt SA
ELL-IN 00 43-N
In Commercial Distribution

  • 07640151088422 ()
ELL-IN 00 43-N

  • Orthopaedic implantable-device cutter
PEDICLE PROBE SMALL
SpineArt SA
ELL-IN 02 23-N
In Commercial Distribution

  • 07640151088347 ()
ELL-IN 02 23-N

  • Bone awl, reusable
PEDICLE PROBE
SpineArt SA
ELL-IN 02 22-N
In Commercial Distribution

  • 07640151088330 ()
ELL-IN 02 22-N

  • Bone awl, reusable
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