Home GUDID 10803622128070 EasyFlow Duo Cannula
Primary DI 10803622128070
Brand EasyFlow Duo Cannula
Company LIVANOVA USA, INC.
Model Duo Cannula
Published 2015-09-17
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 10803622128070 Package GS1 1 In Commercial Distribution 00803622128073 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 10803622128070 10803622128070 00803622128073 00803622128073 803622128073 0803622128073
GMDN Terms# Term, Definition table Term Definition Aorta cannula A sterile, rigid or semi-rigid tube that is surgically inserted into the aorta, typically through the femoral artery and advanced until its distal tip is inside the abdominal aorta, to serve as a channel for the transport of fluid. It may be used for a variety of purposes, e. g, the injection or withdrawal of substances and/or blood, and commonly for external blood circulation during cardiopulmonary bypass procedures or as an outflow for ventricular assist systems. Insertion is achieved with the use of a removable stylet or trocar. 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 00824846005445 NA MEDTRONIC, INC. DWF 2026-07-30 00824846005469 NA MEDTRONIC, INC. DWF 2026-07-30 00824846005667 NA MEDTRONIC, INC. DWF 2026-07-30 00824846006022 NA MEDTRONIC, INC. DWF 2026-07-30 00824846007944 NA MEDTRONIC, INC. DWF 2026-07-30 00840479401096 enableCV Fem-Flex II™ Femoral Arterial Cannula ENABLECV INC. DWF 2026-07-27 00840479401119 enableCV Fem-Flex II™ Femoral Arterial Cannula ENABLECV INC. DWF 2026-07-27 00840479401133 enableCV Fem-Flex II™ Femoral Arterial Cannula ENABLECV INC. DWF 2026-07-27 00840479401157 enableCV Fem-Flex II™ Femoral Arterial Cannula ENABLECV INC. DWF 2026-07-27 00840479401171 enableCV Fem-Flex II™ Femoral Arterial Cannula ENABLECV INC. DWF 2026-07-27 00840479401195 enableCV Fem-Flex II™ Femoral Arterial Cannula ENABLECV INC. DWF 2026-07-27 00824846004721 NA MEDTRONIC, INC. DWF 2026-07-19 00824846004738 NA MEDTRONIC, INC. DWF 2026-07-19 00824846004028 NA MEDTRONIC, INC. DWF 2026-07-16 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