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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Gelweave Siena Ante-flo Pre-Curved Radiopaque
VASCUTEK LTD
735028/10RMSTE
In Commercial Distribution

  • 05037881174853 ()
735028/10RMSTE

  • Synthetic vascular graft
Gelweave Siena Ante-flo Pre-Curved Radiopaque
VASCUTEK LTD
735030/10RMSTE
In Commercial Distribution

  • 05037881174846 ()
735030/10RMSTE

  • Synthetic vascular graft
Gelweave Bifurcate
VASCUTEK LTD
732211E
In Commercial Distribution

  • 05037881174839 ()
732211E

  • Synthetic vascular graft
Gelweave Bifurcate
VASCUTEK LTD
732010E
In Commercial Distribution

  • 05037881174822 ()
732010E

  • Synthetic vascular graft
Gelweave Siena Ante-flo Pre-Curved Radiopaque
VASCUTEK LTD
735032/10RMSTE
In Commercial Distribution

  • 05037881174815 ()
735032/10RMSTE

  • Synthetic vascular graft
Gelweave Siena Ante-flo Pre-Curved Radiopaque
VASCUTEK LTD
735034/10RMSTE
In Commercial Distribution

  • 05037881174808 ()
735034/10RMSTE

  • Synthetic vascular graft
Gelweave Bifurcate
VASCUTEK LTD
731809E
In Commercial Distribution

  • 05037881174792 ()
731809E

  • Synthetic vascular graft
Gelweave Curved Siena Plexus Radiopaque
VASCUTEK LTD
73201088/8RMSTE
In Commercial Distribution

  • 05037881174785 ()
73201088/8RMSTE

  • Synthetic vascular graft
Gelweave Curved Siena Plexus Radiopaque
VASCUTEK LTD
73221088/8RMSTE
In Commercial Distribution

  • 05037881174778 ()
73221088/8RMSTE

  • Synthetic vascular graft
Gelweave Curved Siena Plexus Radiopaque
VASCUTEK LTD
73241088/8RMSTE
In Commercial Distribution

  • 05037881174761 ()
73241088/8RMSTE

  • Synthetic vascular graft
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