Primary Device ID | 00840050510438 |
NIH Device Record Key | 509a7289-c36d-4af4-8f6e-8e48ccfa953b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Discover |
Version Model Number | DIS-SAL-17104 |
Company DUNS | 169065054 |
Company Name | AMERICAN SCREENING, L.L.C. |
Device Count | 1 |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840050510438 [Primary] |
QAW | Test, Tricyclic Antidepressants, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-21 |
Device Publish Date | 2022-11-11 |