Home GUDID 20673978545893 Intersept®
Primary DI 20673978545893
Brand Intersept®
Company MEDTRONIC, INC.
Model 3006
Device description TUBING 3006 3/16x1/16x6 FT
Published 2016-05-28
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
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DWE Tubing, Pump, Cardiopulmonary Bypass Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20673978545893 Package GS1 10 In Commercial Distribution 00673978545899 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 20673978545893 20673978545893 00673978545899 00673978545899 673978545899 0673978545899
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 Device Size Text, specify 0 Device Size Text, specify 0 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 H965252810 AngioVac NAVILYST MEDICAL, INC. DWE 2020-05-11 00616258021539 48” (122 cm) High Pressure Connector Tube BAYER MEDICAL CARE INC. DWE 2019-10-25 00616258008509 48” (122 cm) High Pressure Connector Tube BAYER MEDICAL CARE INC. DWE 2016-12-05 00616258008516 30” (76 cm) High Pressure Connector Tube BAYER MEDICAL CARE INC. DWE 2016-12-05 00616258008523 20” (50 cm) High Pressure Connector Tube BAYER MEDICAL CARE INC. DWE 2016-12-05 00616258008530 10” (25 cm) High Pressure Connector Tube BAYER MEDICAL CARE INC. DWE 2016-12-05 00643169137653 NA MEDTRONIC, INC. DWE 2016-07-23 00613994352811 Intersept® MEDTRONIC, INC. DWE 2016-06-17 00643169169593 NA MEDTRONIC, INC. DWE 2016-06-11 00643169229136 NA MEDTRONIC, INC. DWE 2016-06-11 00643169019287 INTERSEPT® MEDTRONIC, INC. DWE 2016-06-06 00643169029293 NA MEDTRONIC, INC. DWE 2016-06-06 00613994363220 Intersept® MEDTRONIC, INC. DWE 2016-05-28 00613994363237 Intersept® MEDTRONIC, INC. DWE 2016-05-28 00613994407351 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00613994407481 Intersept® MEDTRONIC, INC. DWE 2016-05-28 00613994408426 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00613994408488 Intersept® MEDTRONIC, INC. DWE 2016-05-28 00613994462831 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00613994463494 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00613994851420 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00613994897114 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00613994946317 Intersept® MEDTRONIC, INC. DWE 2016-05-28 00613994946331 Intersept® MEDTRONIC, INC. DWE 2016-05-28 00643169021358 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00643169029125 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00643169061866 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00643169096837 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00643169096905 INTERSEPT® MEDTRONIC, INC. DWE 2016-05-28 00613994097408 NA MEDTRONIC, INC. DWE 2016-05-22
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