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 Pre-Curved Plexus
VASCUTEK LTD
732412810/10STAE
In Commercial Distribution

  • 05037881172897 ()
732412810/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
732612810/10STAE
In Commercial Distribution

  • 05037881172880 ()
732612810/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
732812810/10STAE
In Commercial Distribution

  • 05037881172873 ()
732812810/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
733012810/10STAE
In Commercial Distribution

  • 05037881172866 ()
733012810/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
733212810/10STAE
In Commercial Distribution

  • 05037881172859 ()
733212810/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
733412810/10STAE
In Commercial Distribution

  • 05037881172842 ()
733412810/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
73201088/10STAE
In Commercial Distribution

  • 05037881172835 ()
73201088/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
73221088/10STAE
In Commercial Distribution

  • 05037881172828 ()
73221088/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
73241088/10STAE
In Commercial Distribution

  • 05037881172811 ()
73241088/10STAE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
73261088/10STAE
In Commercial Distribution

  • 05037881172804 ()
73261088/10STAE

  • Synthetic vascular graft
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