Alaris, VeraSafe 10807855

GUDID 50885403234475

Alaris VeraSafe Extension Set

CAREFUSION 303, INC.

Electric infusion pump administration set, single-use
Primary Device ID50885403234475
NIH Device Record Key989a9bad-530a-43c0-8fdc-e57dc875c699
Commercial Distribution StatusIn Commercial Distribution
Brand NameAlaris, VeraSafe
Version Model Number10807855
Catalog Number10807855
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
GS110885403234477 [Unit of Use]
GS150885403234475 [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 Number4
Public Version Date2020-04-27
Device Publish Date2016-12-13

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