Home GUDID 50192253003756 Argyle
Primary DI 50192253003756
Brand Argyle
Company Cardinal Health 200, LLC
Model 8888590216
Catalog number 8888590216
Device description Argyle Left Ventricular Sump Vent Catheter, Catheter Retention Ring, 18 Fr/Ch (6.0 mm) x 20 in. (51 cm)
Published 2025-01-28
Public version status New
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 50192253003756 Package GS1 10 In Commercial Distribution 10192253003758 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 50192253003756 50192253003756 10192253003758 10192253003758
GMDN Terms# Term, Definition table Term Definition Cardiac ventriculography catheter A flexible tube with specific tip configurations designed to enter the left or right ventricle to perform diagnostic haemodynamic/angiographic procedures with contrast media. The distal tip may have an end hole and/or several side holes. The tube is introduced into a peripheral blood vessel and its distal tip is placed in the left or right ventricle according to the desired ventriculography. Left ventriculography is used to assess impairment of the left ventricle, the presence of ventricular aneurysms or septal defects, or to assess the mitral valve. Right ventriculography is used mostly to asses congenital heart disease. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Catheter Gauge 18 French Length 20 Inch
Regulatory Flags# DUNS number 961027315 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 true 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 00199150080649 NA MEDTRONIC, INC. DWF 2026-05-23 00199150080694 NA MEDTRONIC, INC. DWF 2026-05-23 00199150080700 NA MEDTRONIC, INC. DWF 2026-05-23 00199150081004 NA MEDTRONIC, INC. DWF 2026-05-23 00199150081011 NA MEDTRONIC, INC. DWF 2026-05-23 00199150081066 NA MEDTRONIC, INC. DWF 2026-05-23 00199150081714 NA MEDTRONIC, INC. DWF 2026-05-23 00199150081745 NA MEDTRONIC, INC. DWF 2026-05-23 00199150081035 NA MEDTRONIC, INC. DWF 2026-05-22 00199150081042 NA MEDTRONIC, INC. DWF 2026-05-22 00199150081707 NA MEDTRONIC, INC. DWF 2026-05-22 00199150081738 NA MEDTRONIC, INC. DWF 2026-05-22 00199150082902 NA MEDTRONIC, INC. DWF 2026-05-22 20199150073652 NA MEDTRONIC, INC. DWF 2026-03-22 20199150073676 NA MEDTRONIC, INC. DWF 2026-03-22 20199150073690 NA MEDTRONIC, INC. DWF 2026-03-22 00199150073894 NA MEDTRONIC, INC. DWF 2026-03-22 00199150073900 NA MEDTRONIC, INC. DWF 2026-03-22 20199150073928 NA MEDTRONIC, INC. DWF 2026-03-22 20199150074116 NA MEDTRONIC, INC. DWF 2026-03-22 00199150074365 NA MEDTRONIC, INC. DWF 2026-03-22 20763000990286 NA MEDTRONIC, INC. DWF 2026-03-16 00199150071623 NA MEDTRONIC, INC. DWF 2026-03-07 20199150071917 NA MEDTRONIC, INC. DWF 2026-03-07 00199150071920 NA MEDTRONIC, INC. DWF 2026-03-07 00199150071937 NA MEDTRONIC, INC. DWF 2026-03-07 00199150071944 NA MEDTRONIC, INC. DWF 2026-03-07 20199150072020 NA MEDTRONIC, INC. DWF 2026-03-07 00199150072033 NA MEDTRONIC, INC. DWF 2026-03-07 00199150072040 NA MEDTRONIC, INC. DWF 2026-03-07