| Primary Device ID | 00860007588907 |
| NIH Device Record Key | e74758bd-9c3f-4a9d-acc0-a1b5904acf92 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NicCheck I |
| Version Model Number | 1 |
| Catalog Number | 500-001 |
| Company DUNS | 039309062 |
| Company Name | Mossman Associates, Inc. |
| 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 | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00860007588907 [Primary] |
| MRS | Test System, Nicotine, Cotinine, Metabolites |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-07 |
| Device Publish Date | 2022-10-29 |