| Primary Device ID | 10869419000240 |
| NIH Device Record Key | fe5f8b95-1ec7-4a1e-babf-282f5e4290dd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Express ResultsTM |
| Version Model Number | DOA-154-181 |
| Company DUNS | 189222334 |
| Company Name | Quest Diagnostics |
| 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 | 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 | 00869419000243 [Unit of Use] |
| GS1 | 10869419000240 [Primary] |
| LFG | Radioimmunoassay, Tricyclic Antidepressant Drugs |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2021-05-24 |
| Device Publish Date | 2016-09-24 |
| 10869419000240 | DOA-154-181 |
| 10869419000233 | UDOA-12CE-0712-01 |
| 10869419000226 | UDOA-10CE-1307-01 |
| 10869419000219 | UDOA-10CA-0503-01 |
| 10869419000202 | UDOA-6CA-0503-01 |
| 00869419000236 | UDOA-12CE-0712-01 (Ox/Cr/pH)++(OXY/PPX)+(mAMP/MOP/PCP)+(BZO/MTD/BAR)+(AMP/COC/THC)MULTI-DRU |
| 00869419000243 | DOA-154-181(COC/AMP/THC/OPI/PCP)MULTI-DRUG 5 PANEL SCREEN TEST (DOA-154-181) previous (GTIN 1086 |
| 00869419000212 | DUA-1107-061 (Ox/SG/pH)+(mAMP/OPI/PCP)+(BZO/MTD/BAR)+(AMP/COC/THC)+ 5 MULTI-DRUG 10 PANEL U |
| 00869419000205 | DUA-167-012 (Ox/SG/pH)+(mAMP/OPI/PCP)+(AMP/COC/THC)MULTI-DRUG 6 PANEL INTEGRATED CUP WITH previo |