| Primary Device ID | 05206569560015 |
| NIH Device Record Key | 6120298d-49be-4a00-8c73-e76f046bc0a6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BONASIL A+ Putty |
| Version Model Number | Regular Set, 400g Base + 400g Catalyst |
| Catalog Number | 210101800 |
| Company DUNS | 728534814 |
| Company Name | DMP DENTAL INDUSTRY S.A. |
| 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 | 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 |