| Primary Device ID | M944TL011510 |
| NIH Device Record Key | 9c308210-29bb-41ff-a24e-6eba59b3faef |
| Commercial Distribution Discontinuation | 2019-04-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Wexler Surgical, Inc. |
| Version Model Number | TL0115.1 |
| Company DUNS | 024882552 |
| Company Name | WEXLER SURGICAL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 |