Primary Device ID | 00855113008630 |
NIH Device Record Key | a5fe5c5a-7b1d-412d-ab03-7f8bd8124fc3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Longeviti Convenience Kit 2.0 |
Version Model Number | 700072 |
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 | 00855113008630 [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 |
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) |
00855113008623 - ClearFit | 2024-03-25 ClearFit Cover 2.1 (9mm thick) |
00855113008630 - Longeviti Convenience Kit 2.0 | 2024-03-25ClearFit & InvisiShunt Convenience Kit |
00855113008630 - Longeviti Convenience Kit 2.0 | 2024-03-25 ClearFit & InvisiShunt Convenience Kit |
00855113008647 - Longeviti Convenience Kit 3.0 | 2024-03-25 ClearFit & InviShunt Convenience Kit |
00855113008654 - Longeviti Convenience Kit 4.0 | 2024-03-25 ClearFit & InviShunt Convenience Kit |
00855113008661 - Longeviti Convenience Kit 5.0 | 2024-03-25 ClearFit & InvisiShunt Conveniece Kit |