| Primary Device ID | 00851950008147 |
| NIH Device Record Key | 122f1f49-123b-4284-a900-c07f2a42a460 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arvolife |
| Version Model Number | Drug Test Panel |
| Company DUNS | 827033924 |
| Company Name | Clinical Guard |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 | true |