Primary Device ID | 30304879302014 |
NIH Device Record Key | e7fb1165-0c5d-4c3e-b6e6-7ffc66a45602 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sodium Chloride Inhalation Solution, USP 0.9% |
Version Model Number | 930201 |
Catalog Number | 0487-9302-01 |
Company DUNS | 079160190 |
Company Name | NEPHRON PHARMACEUTICALS |
Device Count | 25 |
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 | true |
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 |