| Primary Device ID | B36511218L0 |
| NIH Device Record Key | 1f94c820-031d-4fe7-8d67-569a88d9131a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mesh Insert, Carbon Fiber, Side Opening, Long Vers |
| Version Model Number | 11-218-L |
| Company DUNS | 787178920 |
| Company Name | Aktina Corp. |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |