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
732012810/10STDE
In Commercial Distribution

  • 05037881172613 ()
732012810/10STDE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
732212810/10STDE
In Commercial Distribution

  • 05037881172606 ()
732212810/10STDE

  • Synthetic vascular graft
Gelweave Pre-Curved Plexus
VASCUTEK LTD
732412810/10STDE
In Commercial Distribution

  • 05037881172590 ()
732412810/10STDE

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

  • 05037881172583 ()
732612810/10STDE

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

  • 05037881172576 ()
732812810/10STDE

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

  • 05037881172569 ()
733012810/10STDE

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

  • 05037881172552 ()
733212810/10STDE

  • Synthetic vascular graft
Gelweave Ante-Flo
VASCUTEK LTD
734018/8E
In Commercial Distribution

  • 05037881172545 ()
734018/8E

  • Synthetic vascular graft
Gelweave Ante-Flo
VASCUTEK LTD
734020/8E
In Commercial Distribution

  • 05037881172538 ()
734020/8E

  • Synthetic vascular graft
Gelweave Ante-Flo
VASCUTEK LTD
734022/8E
In Commercial Distribution

  • 05037881172521 ()
734022/8E

  • Synthetic vascular graft
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