| Primary Device ID | 00840277404626 |
| NIH Device Record Key | e0f4fe90-a532-48db-a485-a27abcea137a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FairFix CL |
| Version Model Number | 05.05.0145 |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, 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 | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840277404626 [Primary] |
| MBI | Fastener, Fixation, Nondegradable, Soft Tissue |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-25 |
| Device Publish Date | 2024-04-17 |
| 00840277404626 | Continuous Loop with Titanium Button |
| 00840277404619 | Continuous Loop with Titanium Button |
| 00840277404602 | Continuous Loop with Titanium Button |
| 00840277404596 | Continuous Loop with Titanium Button |
| 00840277404589 | Continuous Loop with Titanium Button |
| 00840277404572 | Continuous Loop with Titanium Button |
| 00840277404565 | Continuous Loop with Titanium Button |
| 00840277404558 | Continuous Loop with Titanium Button |
| 00840277404541 | Continuous Loop with Titanium Button |
| 00840277404534 | Continuous Loop with Titanium Button |
| 00840277404527 | Continuous Loop with Titanium Button |