| Primary Device ID | 00855113008661 |
| NIH Device Record Key | ea128170-5829-4975-bae0-c70435c29d23 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Longeviti Convenience Kit 5.0 |
| Version Model Number | 700075 |
| Company DUNS | 070659539 |
| Company Name | LONGEVITI NEURO SOLUTIONS 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 | true |
| 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 | 00855113008661 [Primary] |
| KKY | Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-25 |
| Device Publish Date | 2024-03-15 |
| 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 |
| 00855113008739 - ClearFit | 2024-11-28 ClearFit complex for international sales |
| 00855113008746 - ClearFit | 2024-11-28 ClearFit large for international sales |
| 00855113008715 - ClearFit | 2024-03-28 ClearFit 1.4cm Cover |
| 00855113008722 - ClearFit | 2024-03-28 ClearFit 1.4cm Cover with Slot |
| 00855113008562 - ClearFit | 2024-03-25 ClearFit Cover 2.0 (5.7mm thick) |