Home GUDID 00763000946494 DLP®
Primary DI 00763000946494
Brand DLP®
Company MEDTRONIC, INC.
Model 57417
Device description CANNULA 57417 FEMORAL ART 17FR 4PK 17L
Published 2024-09-27
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
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 20763000946498 Primary GS1 0 00763000946494 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 20763000946498 20763000946498 00763000946494 00763000946494 763000946494 0763000946494
GMDN Terms# Term, Definition table Term Definition Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return A semi-rigid or rigid tube intended to be surgically inserted into an artery or vein to serve as a channel for the extracorporeal transport of oxygenated blood to a patient during cardiopulmonary bypass and/or extracorporeal membrane oxygenation; in some settings it may be referred to as an arterial cannula. It is typically inserted using a compatible trocar blade which may be included. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Catheter Gauge 17 French
Regulatory Flags# DUNS number 006261481 Device count 4 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 false 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
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