Home GUDID 20801902140573 ARROW
Primary DI 20801902140573
Brand ARROW
Company TELEFLEX INCORPORATED
Model IPN036616
Catalog number CDC-12702-B1A
Device description Two-Lumen CVC Kit
Published 2018-04-13
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true Product Codes# Code, Name table Code Name DQY Catheter, percutaneous
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DQY Catheter, Percutaneous Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20801902116745 Package GS1 5 Not in Commercial Distribution 20801902140573 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 20801902116745 20801902116745 20801902140573 20801902140573
GMDN Terms# Term, Definition table Term Definition Centrally-inserted central venous catheter A flexible tube intended to be introduced into a neck or thoracic vein and often advanced into the superior vena cava for various infusion/aspiration procedures (i.e., non-dedicated) including the intravenous administration of nutrients, fluids, chemotherapeutic agents or other drugs, and blood sampling or delivery; it may also be used to monitor venous pressure. The proximal end of this central venous catheter (CVC) is typically fixed to the patient for long-term use. It may include supportive devices associated with introduction (e.g., guidewire, introducer); it is not primarily intended for extracorporeal blood therapies such as haemodialysis. This is a single-use device.
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Store between 20 - 25°C (68 - 77°F). Storage Environment Temperature 20 Degrees Celsius 25 Degrees Celsius
Regulatory Flags# DUNS number 002348191 Device count 1 Kit true Combination product true Lot or batch true Expiration date on label true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 07613327623338 AXS Lift Stryker Corporation DQY 2025-03-04 07613327623376 AXS Lift Stryker Corporation DQY 2025-03-04 07613327417203 AXS Catalyst 7 Stryker Corporation DQY 2019-05-13 07613327417227 AXS Catalyst 7 Stryker Corporation DQY 2019-05-13 07613327313888 DAC 038 Stryker Corporation DQY 2016-09-21 07613327313901 DAC 057 Stryker Corporation DQY 2016-09-21 07613327313932 DAC 070 Stryker Corporation DQY 2016-09-21 07613327313949 DAC 057 Stryker Corporation DQY 2016-09-21 08033477054322 Pacific™ Plus MEDTRONIC, INC. DQY 2016-06-26 08033477054360 Pacific™ Plus MEDTRONIC, INC. DQY 2016-06-26 08033477054384 Pacific™ Plus MEDTRONIC, INC. DQY 2016-06-26 08033477054391 Pacific™ Plus MEDTRONIC, INC. DQY 2016-06-26 08033477054407 Pacific™ Plus MEDTRONIC, INC. DQY 2016-06-26 08033477054421 Pacific™ Plus MEDTRONIC, INC. DQY 2016-06-26 08033477054438 Pacific™ Plus MEDTRONIC, INC. DQY 2016-06-26 08033477048772 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477048802 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477048833 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477048864 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477048888 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477048925 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477048956 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477048987 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477049014 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477049045 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477049069 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477049076 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477049106 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477049137 REEF HP MEDTRONIC, INC. DQY 2016-06-19 08033477049168 REEF HP MEDTRONIC, INC. DQY 2016-06-19
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