Home GUDID 00690103026849
EDWARDS LIFESCIENCES PERIPHERAL GUIDEWIRE
Primary DI 00690103026849
Brand EDWARDS LIFESCIENCES PERIPHERAL GUIDEWIRE
Company Edwards Lifesciences LLC
Model ART100
Catalog number ART100
Device description PERIPHERAL GUIDEWIRE
Published 2016-08-31
Public version status Update
Distribution status 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 50690103026844 Package GS1 10 In Commercial Distribution 00690103026849 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 50690103026844 50690103026844 00690103026849 00690103026849 690103026849 0690103026849
GMDN Terms# Term, Definition table Term Definition Cardiac/peripheral vascular guidewire, single-use A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). 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 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 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