Home GUDID B1521580F075MM750 PEMCO INC
Primary DI B1521580F075MM750
Brand PEMCO INC
Company PEMCO INC
Model 1580-F-07-5MM-75
Catalog number 1580-F-07-5MM-75
Device description Perfusion Cannula. Flag Handle 6.5 inches long. Style # 7 Swivel Tip - 5 MM Tip Diameter. 75 Degree Bend. Also available in: Large, Small, & Tube H
Published 2016-09-26
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile false
Single use false 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 B1521580F075MM750 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Vascular irrigation cannula, coronary artery, reusable A rigid or semi-rigid tube designed to be surgically inserted, temporarily, into a coronary artery to serve as a channel for the transport of fluid during a surgical intervention. It is typically intended for the infusion and/or perfusion of fluids in diagnostic and/or surgical procedures, such as cardiopulmonary bypass, and to help avoid ischemia. Insertion is typically achieved with the use of a removable stylet or trocar blade. This is a reusable device intended to be sterilized prior to use.
Device Sizes# Type, Value, Unit table Type Value Unit Angle 75 degree Length 6.5 Inch Outer Diameter 5 Millimeter
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 004217071 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 true Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true 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