| Primary Device ID | 00850557007584 |
| NIH Device Record Key | e725a8fa-223f-46d0-9b11-50c411838aa8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ten Panel PreScreen Plus Cup (CLIA Waived) |
| Version Model Number | PSC-DOA-4104 |
| 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 | 00850557007584 [Primary] |
| GS1 | 00850557007591 [Package] Package: Inner Pack [25 Units] In Commercial Distribution |
| GS1 | 10850557007598 [Package] Contains: 00850557007591 Package: Case [4 Units] In Commercial Distribution |
| LDJ | Enzyme Immunoassay, Cannabinoids |
| 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 | 2016-07-25 |
| 00850557007669 | Ten Panel PreScreen Plus Cup (CLIA Waived) Drug Combo: THC | COC | OPI | mAMP | AMP | BZO | MTD |
| 00850557007621 | Ten Panel PreScreen Plus Cup (CLIA Waived) Drug Combo: BAR | BUP | BZO | COC | MET | MTD | OPI | |
| 00850557007584 | Ten Panel PreScreen Plus Cup (CLIA Waived) Drug Combo: AMP | BAR | BZO | COC | MET | MTD | OPI | |
| 00850557007508 | Ten Panel PreScreen Plus Cup (CLIA Waived) Drug Combo: AMP | BAR | BZO | COC | MDMA | MET | MTD |