| Primary Device ID | D9671800403 |
| NIH Device Record Key | 77881faa-c743-4779-90b7-7f749788e97c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Prevest Surgical Guide 3D Printing Resin |
| Version Model Number | 1000g plastic bottle |
| Catalog Number | 18004 |
| Company DUNS | 859546940 |
| Company Name | PREVEST DENPRO LIMITED |
| 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 | 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 | true |