Primary Device ID | 50885403221703 |
NIH Device Record Key | 80b4ff5b-5a98-42d2-a3d1-f541495f589d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Alaris, Texium |
Version Model Number | 10012241-0500 |
Catalog Number | 10012241-0500 |
Company DUNS | 360624720 |
Company Name | CAREFUSION 303, INC. |
Device Count | 100 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)854-7128 |
CustCareInfusion@carefusion.com | |
Phone | +1(800)854-7128 |
CustCareInfusion@carefusion.com |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 125 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 125 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10885403221705 [Unit of Use] |
GS1 | 50885403221703 [Primary] |
FPA | Set, administration, intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-04-27 |
Device Publish Date | 2016-09-22 |
50885403239593 | Alaris Pump Module Texium Low Sorbing Infusion Set |
50885403229921 | Alaris Texium Secondary Set |
50885403225626 | Alaris Texium Secondary Set |
50885403221703 | Alaris Texium closed male luer |