Home GUDID 10803622136365
EasyFlow Duo Cannula
Primary DI 10803622136365
Brand EasyFlow Duo Cannula
Company LIVANOVA USA, INC.
Model Duo Cannula
Published 2017-06-14
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
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 10803622136365 Package GS1 5 In Commercial Distribution 00803622136368 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 10803622136365 10803622136365 00803622136368 00803622136368 803622136368 0803622136368
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.
Regulatory Flags# DUNS number 080914995 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 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 00199150083817 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083893 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083985 NA MEDTRONIC, INC. DWF 2026-05-30 18051160302878 Quantum SuperPAC Tubing Set - SP05E-BB SPECTRUM MEDICAL SRL DWF 2026-05-27 00199150078455 NA MEDTRONIC, INC. DWF 2026-04-26 08033178017190 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017206 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017213 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017220 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017237 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017244 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017251 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017268 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11