Home GUDID 20673978546319 Intersept®
Primary DI 20673978546319
Brand Intersept®
Company MEDTRONIC, INC.
Model 3606
Device description TUBING 3606 1/2x3/32x6 FT
Published 2016-06-16
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 DWE TUBING, PUMP, CARDIOPULMONARY BYPASS KMF Bandage, liquid
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DWE Tubing, Pump, Cardiopulmonary Bypass Cardiovascular 2 KMF Bandage, Liquid General Hospital 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20673978546319 Package GS1 10 In Commercial Distribution 00673978546315 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 20673978546319 20673978546319 00673978546315 00673978546315 673978546315 0673978546315
GMDN Terms# Term, Definition table Term Definition Cardiopulmonary bypass system tubing set A collection of sterile devices including tubing and typically clamps, filters, connectors, and stopcocks, used in a circuit for a cardiopulmonary bypass procedure. The tubing is typically polymeric and may be heparin coated. It is typically used in the blood pump head of a cardiopulmonary bypass system. The tubing, when used in a roller type pump, will be cyclically compressed by the blood pump to cause the blood to flow through the heart-lung bypass system. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Length 1.8 Meter
Regulatory Flags# DUNS number 006261481 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 false 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 00803622164019 Perfusion Pack LIVANOVA USA, INC. DWE 2026-06-26 10192253047981 Kendall Cardinal Health 200, LLC KMF 2026-06-09 10192253047998 Kendall Cardinal Health 200, LLC KMF 2026-06-09 10192253048001 Kendall Cardinal Health 200, LLC KMF 2026-06-09 10192253048018 Kendall Cardinal Health 200, LLC KMF 2026-06-09 10192253048025 Kendall Cardinal Health 200, LLC KMF 2026-06-09 10192253048032 Kendall Cardinal Health 200, LLC KMF 2026-06-09 10192253047974 Kendall Cardinal Health 200, LLC KMF 2026-05-13 10192253047943 Kendall Cardinal Health 200, LLC KMF 2026-05-12 10192253047950 Kendall Cardinal Health 200, LLC KMF 2026-05-12 10888277719743 Medline MEDLINE INDUSTRIES, INC. KMF 2024-03-05 10192253048087 Kendall Cardinal Health 200, LLC KMF 2024-03-04 10192253048094 Kendall Cardinal Health 200, LLC KMF 2024-03-04 10192253048100 Kendall Cardinal Health 200, LLC KMF 2024-03-04 10192253048117 Kendall Cardinal Health 200, LLC KMF 2024-03-04 10192253046908 Curity Cardinal Health 200, LLC KMF 2023-11-03 10192253046861 Curity Cardinal Health 200, LLC KMF 2023-10-25 10192253046885 Curity Cardinal Health 200, LLC KMF 2023-10-25 20192253046875 Curity Cardinal Health 200, LLC KMF 2023-10-25 10192253046847 Curity Cardinal Health 200, LLC KMF 2023-10-24 10192253046854 Curity Cardinal Health 200, LLC KMF 2023-10-24 50707387809916 3M™ Cavilon™ 3M COMPANY KMF 2023-09-22 08711428065947 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08 08711428076820 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08 10707387793231 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08 10707387810679 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08 50707387809589 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08 50707387809671 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08 50707387809688 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08 50707387809695 3M™ Cavilon™ 3M COMPANY KMF 2023-06-08
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