| Primary Device ID | H668092160P1 |
| NIH Device Record Key | 4a6b3db3-bb37-43dd-b3db-686505ebce4f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bosworth Tru Repair |
| Version Model Number | 092160P |
| Catalog Number | 092160P |
| Company DUNS | 014769301 |
| Company Name | Harry J Bosworth Company |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| 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 |