| Primary Device ID | 00860004081661 |
| NIH Device Record Key | 3beae78b-03dd-41b9-b694-5813bf89f1f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | P33 |
| Version Model Number | P33-10-MET |
| Catalog Number | P33-10-MET |
| Company DUNS | 086645029 |
| Company Name | DEUS VULT, LLC |
| 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 | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860004081647 [Unit of Use] |
| GS1 | 00860004081654 [Primary] |
| GS1 | 00860004081661 [Package] Contains: 00860004081654 Package: case [4 Units] In Commercial Distribution |
| NFT | Test, Amphetamine, 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 | 2022-01-07 |
| Device Publish Date | 2021-12-30 |
| 00850040879162 - Number 1 | 2024-02-09 12-Panel Drug Test Cup: AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, PCP, TCA, THC |
| 00860004081661 - P33 | 2022-01-0710 Panel Drug Test Cup – AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, THC |
| 00860004081661 - P33 | 2022-01-07 10 Panel Drug Test Cup – AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, THC |
| 00860004081609 - Preferred Med Supply | 2021-08-19 Multi-panel Drug Test Cup |