Home GUDID 10801741090216 BARD® BURBANK
Primary DI 10801741090216
Brand BARD® BURBANK
Company Bard Peripheral Vascular, Inc.
Model SGA150001
Catalog number SGA150001
Device description BARD® BURBANK™ Carotid Bypass Shunt, 12F - 9F x 15.5cm
Published 2016-09-19
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 10801741090216 Package GS1 5 In Commercial Distribution 00801741090219 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 10801741090216 10801741090216 00801741090219 00801741090219 801741090219 0801741090219
GMDN Terms# Term, Definition table Term Definition Carotid artery shunt A sterile device designed to serve as a temporary blood conduit (a shunt) connecting the distal internal carotid artery to the proximal common carotid artery allowing intravascular blood to continuously flow to the patient's brain during an endarterectomy procedure. It is typically designed as a hollow shaft with atraumatic dilations (e.g., balloons) on either end. The shaft is inserted into the lumen of the blood vessel, via a small incision at the surgical site. It is typically made of silicone elastomer and polyester radiopaque materials and is available in a range of diameters. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Length 15.5 Centimeter
Regulatory Flags# DUNS number 135057938 Device count 1 DM exempt false Premarket exempt true 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 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