Primary Device ID | 50885403234475 |
NIH Device Record Key | 989a9bad-530a-43c0-8fdc-e57dc875c699 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Alaris, VeraSafe |
Version Model Number | 10807855 |
Catalog Number | 10807855 |
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 | 10885403234477 [Unit of Use] |
GS1 | 50885403234475 [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 | 4 |
Public Version Date | 2020-04-27 |
Device Publish Date | 2016-12-13 |
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