Home GUDID B0663010270006 42" .165 x .230 Perfusion Adaprot Set w/Clear 3/8"
Primary DI B0663010270006
Brand 42" .165 x .230 Perfusion Adaprot Set w/Clear 3/8"
Company NOVOSCI CORP.
Model 301027-000
Catalog number 301027-000
Device description A sterile device designed to facilitate/regulate the delivery of cardioplegic solution to the heart during a cardiopulmonary bypass procedure by conne
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 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 B0663010270003 Package HIBCC 25 In Commercial Distribution B0663010270004 Package HIBCC 50 In Commercial Distribution B0663010270005 Package HIBCC 75 In Commercial Distribution B0663010270006 Package HIBCC 100 In Commercial Distribution B0663010270000 Primary HIBCC 0
GMDN Terms# Term, Definition table Term Definition Cardioplegia solution administration adaptor A sterile device designed to facilitate/regulate the delivery of cardioplegic solution to the heart during a cardiopulmonary bypass procedure by connecting an administration line to a cardioplegia cannula. Also known as a cardioplegia delivery set, it basically consists of tubing [e.g., polyvinyl chloride (PVC)] with connectors. It may have a single lumen or branched multiple-lumen design and include various types of connectors, clamps, and valves, depending on additional intended uses (e.g., venting, recirculation, and/or simultaneous perfusion of vein grafts). This is a single-use device.
Regulatory Flags# DUNS number 938289980 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 true 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# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published B0662010110000 STOPCOCK, TMP 3-WAY W/LUER LOCK 201011-000 201011-000 2015-09-14 B0662010120000 STOPCOCK, TMP 4-WAY W/LUER LOCK 201012-000 201012-000 2015-09-14 B0663110330000 TUBING ORGANIZER - STERILE 311033-000 311033-000 2015-10-06 B066311033NS1 TUBING ORGANIZER - NON-STERILE 311033NS 311033NS 2015-10-13 B0663110340000 PEDIATRIC TUBING ORGANIZER - STERILE 311034-000 311034-000 2015-10-12 B066311034NS1 PEDIATRIC TUBING ORGANIZRER - NON-STERILE 311034NS 311034NS 2015-10-13 B066321244NS1 "CONNECTOR, 1/4"" X 1/2"" X 1/2"" CLEAR PAY " 321244NS 321244NS 2015-10-13 B066201006NS1 CANNULAE, SAPHENOUS VEIN 201006NS 201006NS 2015-11-11 B066301011NS1 "QUICKIE PRIME - 1/4"" x 1/16""" 301011NS 301011NS 2017-12-06 B066331011NS1 "CONNECTOR, 3/16"" X 3/16"" W/OUT PART LINE " 331011NS 331011NS 2015-10-13 B066331012NS1 "CONNECTOR, 3/16"" X 1/4"" W/OUT PART LINE" 331012NS 331012NS 2015-10-13 B066331022NS1 "CONNECTOR, 1/4"" X 1/4"" W/OUT PART LINE" 331022NS 331022NS 2015-10-13 B066331023NS1 "CONNECTOR, 1/4"" X 3/8"" W/OUT PART LINE" 331023NS 331023NS 2015-10-13 B066331024NS1 "CONNECTOR, 1/4"" X 1/2"" W/OUT LUER " 331024NS 331024NS 2015-10-13 B066331033NS1 "CONNECTOR, 3/8"" X 3/8"" W/OUT PART LINE" 331033NS 331033NS 2015-10-13 B066331034NS1 "CONNECTOR, 3/8"" X 1/2"" W/OUT PART LINE" 331034NS 331034NS 2015-10-13 B066331044NS1 "CONNECTOR, 1/2"" X 1/2"" W/OUT PART LINE" 331044NS 331044NS 2015-10-13 B066332011NS1 "CONNECTOR, 3/16"" X 3/16"" W/OUT PART LINE W/LUER" 332011NS 332011NS 2015-10-13 B066332012NS1 "CONNECTOR, 3/16"" X 1/4"" W/OUT PART LINE W/LUER" 332012NS 332012NS 2015-10-13 B066332022NS1 "CONNECTOR, 1/4"" X 1/4"" W/LUER" 332022NS 332022NS 2015-10-13
Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 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 00199150083800 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083817 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083893 NA MEDTRONIC, INC. DWF 2026-05-30 00199150083985 NA MEDTRONIC, INC. DWF 2026-05-30 18051160302878 Quantum SuperPAC Tubing Set - SP05E-BB SPECTRUM MEDICAL SRL DWF 2026-05-27 00199150078455 NA MEDTRONIC, INC. DWF 2026-04-26 08033178017190 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017206 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017213 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017220 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017237 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017244 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017251 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11 08033178017268 Cardioplegia Cannula SORIN GROUP ITALIA SRL DWF 2026-02-11
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