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 Trifurcate Arch
VASCUTEK LTD
732014/8X2E
In Commercial Distribution

  • 05037881171739 ()
732014/8X2E

  • Synthetic vascular graft
Gelweave Trifurcate Arch
VASCUTEK LTD
732014/10X2E
In Commercial Distribution

  • 05037881171722 ()
732014/10X2E

  • Synthetic vascular graft
Gelweave Thoracic Arch
VASCUTEK LTD
732212/10/8AE
In Commercial Distribution

  • 05037881171715 ()
732212/10/8AE

  • Synthetic vascular graft
Gelweave Thoracic Arch
VASCUTEK LTD
732214/10/10AE
In Commercial Distribution

  • 05037881171708 ()
732214/10/10AE

  • Synthetic vascular graft
Gelweave Thoracic Arch Radiopaque
VASCUTEK LTD
732212/10/8ARME
In Commercial Distribution

  • 05037881171692 ()
732212/10/8ARME

  • Synthetic vascular graft
Gelweave Thoracic Arch Radiopaque
VASCUTEK LTD
732214/10/10ARME
In Commercial Distribution

  • 05037881171685 ()
732214/10/10ARME

  • Synthetic vascular graft
Gelweave Thoracic Arch Radiopaque
VASCUTEK LTD
732212/10/8CRME
In Commercial Distribution

  • 05037881171678 ()
732212/10/8CRME

  • Synthetic vascular graft
Gelweave Thoracic Arch Radiopaque
VASCUTEK LTD
732214/10/10CRME
In Commercial Distribution

  • 05037881171661 ()
732214/10/10CRME

  • Synthetic vascular graft
Gelweave Double Bifurcate Radiopaque
VASCUTEK LTD
731407/6x2RME
In Commercial Distribution

  • 05037881171654 ()
731407/6x2RME

  • Synthetic vascular graft
Gelweave Double Bifurcate Radiopaque
VASCUTEK LTD
731608/7x2RME
In Commercial Distribution

  • 05037881171647 ()
731608/7x2RME

  • Synthetic vascular graft
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