| Primary Device ID | 00670082000368 |
| NIH Device Record Key | 4a39ccab-5697-46c3-8952-1a7312e9771d |
| Commercial Distribution Discontinuation | 2019-08-06 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | BrightMatter Plan |
| Version Model Number | 1.5 |
| Catalog Number | SYN-0004 |
| Company DUNS | 203061833 |
| Company Name | Synaptive Medical 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 | false |
| Lot Batch | true |
| 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 | true |
| OTC Over-The-Counter | false |