| Primary Device ID | 00860003416303 |
| NIH Device Record Key | 85e18b07-0d82-4b2c-8e3e-bc74caf68722 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ClearFit VDI Standard |
| Version Model Number | 171716 |
| Company DUNS | 070659539 |
| Company Name | LONGEVITI NEURO SOLUTIONS LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860003416303 [Primary] |
| GXN | Plate, Cranioplasty, Preformed, Non-Alterable |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-27 |
| Device Publish Date | 2025-02-19 |
| 00855113008579 - ClearFit Posterior Fossa Plate | 2025-02-27 ClearFit Posterior Fossa Plate |
| 00855113008586 - ClearFit Retrosigmoid Large | 2025-02-27 ClearFit Retrosigmoid Large |
| 00855113008753 - ClearFit Retrosigmoid Small | 2025-02-27 ClearFit Retrosigmoid Small |
| 00860003416303 - ClearFit VDI Standard | 2025-02-27ClearFit VDI Standard |
| 00860003416303 - ClearFit VDI Standard | 2025-02-27 ClearFit VDI Standard |
| 00860003416310 - ClearFit VDI Large | 2025-02-27 ClearFit VDI Large |
| 00855113008166 - ClearFit | 2024-11-28 ClearFit small for international sales |
| 00855113008173 - ClearFit | 2024-11-28 ClearFit medium for international sales |
| 00855113008197 - ClearFit | 2024-11-28 ClearFit X-Large for international sales |