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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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SILHOUETTE 2,ACCESSORY Package
PARKER-HANNIFIN CORPORATION
SIL2-ADPT-PKG
Not in Commercial Distribution

  • 00816711024163 ()
SIL2-ADPT-PKG

  • Anaesthesia face mask, reusable
Silhouette 2 Variety Pack
PARKER-HANNIFIN CORPORATION
SIL2-VAR-4x3
In Commercial Distribution

  • 00816711024033 ()
SIL2-VAR-4x3

  • Anaesthesia breathing circuit, single-use
BAG,2 LITER,NON-LATEX
PARKER-HANNIFIN CORPORATION
4100-2NL
In Commercial Distribution

  • 00816711020868 ()
4100-2NL

  • Breathing circuit bag, reusable
2 CYL.CART (N2O REGULATOR) - This is an accessory only; not a medical device
PARKER-HANNIFIN CORPORATION
2100-N
In Commercial Distribution

  • 00816711020585 ()


  • Gas cylinder trolley
2 CYL.CART (LESS REGULATOR) - This is an accessory only; not a medical device
PARKER-HANNIFIN CORPORATION
2100
In Commercial Distribution

  • 00816711020578 ()


  • Gas cylinder trolley
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
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