| Primary Device ID | 00369771000832 |
| NIH Device Record Key | d364c0d3-2570-43b2-b104-6345bcbcf9b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Syringes Safety |
| Version Model Number | 11466 |
| Company DUNS | 361663839 |
| Company Name | GERI-GENTLE CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |