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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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Bander Ureteral Diversion Stent Set Wire Guide With Hydrophilic Coating
COOK INCORPORATED
G15878
In Commercial Distribution

  • 00827002158788 ()
025717

  • Polymeric ureteral stent
Bander Ureteral Diversion Stent Set Wire Guide With Hydrophilic Coating
COOK INCORPORATED
G15877
In Commercial Distribution

  • 00827002158771 ()
025818

  • Polymeric ureteral stent
Bander Ureteral Diversion Stent Set Wire Guide With Hydrophilic Coating
COOK INCORPORATED
G15876
In Commercial Distribution

  • 00827002158764 ()
025817

  • Polymeric ureteral stent
Bander Ureteral Diversion Stent Set Wire Guide With Hydrophilic Coating
COOK INCORPORATED
G15875
In Commercial Distribution

  • 00827002158757 ()
025718

  • Polymeric ureteral stent
Dretler Ureteroscopy Stent Set
COOK INCORPORATED
G15735
In Commercial Distribution

  • 00827002157354 ()
025506-S4

  • Polymeric ureteral stent
Bander Ureteral Diversion Stent Set
COOK INCORPORATED
G15473
In Commercial Distribution

  • 00827002154735 ()
025808

  • Polymeric ureteral stent
Bander Ureteral Diversion Stent Set
COOK INCORPORATED
G15224
In Commercial Distribution

  • 00827002152243 ()
025806

  • Polymeric ureteral stent
Bander Ureteral Diversion Stent Set
COOK INCORPORATED
G15223
In Commercial Distribution

  • 00827002152236 ()
025706

  • Polymeric ureteral stent
VIPER F2 FACET FIXATION SYSTEM SCREW 6 x 60mm
Medos International Sàrl
175710660
Not in Commercial Distribution

  • 10705034034959 ()
175710660

  • Bone-screw internal spinal fixation system, non-sterile
VIPER F2 FACET FIXATION SYSTEM SCREW 6 x 55mm
Medos International Sàrl
175710655
Not in Commercial Distribution

  • 10705034034942 ()
175710655

  • Bone-screw internal spinal fixation system, non-sterile
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