| Primary Device ID | 10851000007110 |
| NIH Device Record Key | 07a0835c-2950-4aa9-bb73-35c55032a822 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived) |
| Version Model Number | PSC-DOA-7125AD |
| Company DUNS | 065602744 |
| Company Name | MERGERS MARKETING, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 00851000007106 [Primary] |
| GS1 | 00851000007113 [Package] Contains: 00851000007106 Package: Inner Pack [25 Units] In Commercial Distribution |
| GS1 | 10851000007110 [Package] Contains: 00851000007113 Package: Case [4 Units] In Commercial Distribution |
| LFG | Radioimmunoassay, Tricyclic Antidepressant Drugs |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-26 |
| 10851000007110 | Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP | BAR | BZO | COC |
| 00850557007706 | Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP | BAR | BUP | BZO |