Home GUDID 00690103026320
Edwards Lifesciences Arterial Perfusion Cannula
Primary DI 00690103026320
Brand Edwards Lifesciences Arterial Perfusion Cannula
Company Edwards Lifesciences LLC
Model APC018
Catalog number APC018
Device description Arterial Perfusion Cannula
Published 2016-08-31
Public version status Update
Distribution status Not in Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true
Product Codes# Code, Name table Code Name DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 50690103026325 Package GS1 10 Not in Commercial Distribution 00690103026320 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 50690103026325 50690103026325 00690103026320 00690103026320 690103026320 0690103026320
GMDN Terms# Term, Definition table Term Definition Cardiopulmonary bypass cannula, arterial A sterile, semi-rigid or rigid tube intended to be used during open heart surgery where it is surgically inserted for perfusion of the ascending aorta, serving as a channel for the transport of pumped, oxygenated, blood from a cardiopulmonary bypass system (heart-lung machine) tubing circuit. It is typically a moulded plastic tube with stainless steel wire reinforcement, to prevent kinking/collapse, having multiple perforations or flutes at the distal end which help diffuse and disperse incoming blood. It may be inserted using a compatible trocar. Some types may be heparin coated and include a pressure monitoring port. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Device Size Text, specify 0
Regulatory Flags# DUNS number 134139174 Device count 1 Lot or batch true Expiration date on label true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00824846003151 NA MEDTRONIC, INC. DWF 2026-07-09 00840479401416 enableCV EZ Glide Aortic Cannula ENABLECV INC. DWF 2026-07-09 00840479401430 enableCV EZ Glide Aortic Cannula ENABLECV INC. DWF 2026-07-09 00824846003472 NA MEDTRONIC, INC. DWF 2026-07-04 00824846003687 NA MEDTRONIC, INC. DWF 2026-07-04 00824846003700 NA MEDTRONIC, INC. DWF 2026-07-04 00824846001669 NA MEDTRONIC, INC. DWF 2026-06-28 00824846001843 NA MEDTRONIC, INC. DWF 2026-06-28 00824846001850 NA MEDTRONIC, INC. DWF 2026-06-28 00840479402222 enableCV Percutaneous Insertion Kit-Arterial ENABLECV INC. DWF 2026-06-26 00824846001614 NA MEDTRONIC, INC. DWF 2026-06-25 08033178019378 Protek Duo SORIN GROUP ITALIA SRL DWF 2026-06-25 08033178019385 Protek Duo SORIN GROUP ITALIA SRL DWF 2026-06-25 00199150083855 NA MEDTRONIC, INC. DWF 2026-06-08 00199150083992 NA MEDTRONIC, INC. DWF 2026-06-08 00199150084180 NA MEDTRONIC, INC. DWF 2026-06-08 00824846000020 NA MEDTRONIC, INC. DWF 2026-06-08 00824846000983 NA MEDTRONIC, INC. DWF 2026-06-08 00824846001027 NA MEDTRONIC, INC. DWF 2026-06-08 00824846001041 NA MEDTRONIC, INC. DWF 2026-06-08 00824846001065 NA MEDTRONIC, INC. DWF 2026-06-08 00199150083077 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083121 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083381 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083442 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083534 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083718 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083763 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083794 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083800 NA MEDTRONIC, INC. DWF 2026-05-30