| Primary Device ID | 00850033629323 |
| NIH Device Record Key | bb199385-e541-4acc-9d4b-ed1e167df31e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DJF Med |
| Version Model Number | DJF1000FS |
| Company DUNS | 117299766 |
| Company Name | Acta Medical LLC |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |