Alaris, Texium 10012241-0500

GUDID 50885403221703

Alaris Texium closed male luer

CAREFUSION 303, INC.

Luer/Luer linear connector, single-use Luer/Luer linear connector, single-use
Primary Device ID50885403221703
NIH Device Record Key80b4ff5b-5a98-42d2-a3d1-f541495f589d
Commercial Distribution StatusIn Commercial Distribution
Brand NameAlaris, Texium
Version Model Number10012241-0500
Catalog Number10012241-0500
Company DUNS360624720
Company NameCAREFUSION 303, INC.
Device Count100
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)854-7128
EmailCustCareInfusion@carefusion.com
Phone+1(800)854-7128
EmailCustCareInfusion@carefusion.com

Operating and Storage Conditions

Storage Environment TemperatureBetween -40 Degrees Fahrenheit and 125 Degrees Fahrenheit
Storage Environment TemperatureBetween -40 Degrees Fahrenheit and 125 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS110885403221705 [Unit of Use]
GS150885403221703 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FPASet, administration, intravascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-04-27
Device Publish Date2016-09-22

On-Brand Devices [Alaris, Texium]

50885403239593Alaris Pump Module Texium Low Sorbing Infusion Set
50885403229921Alaris Texium Secondary Set
50885403225626Alaris Texium Secondary Set
50885403221703Alaris Texium closed male luer

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