| Primary Device ID | D9560000ULB2 |
| NIH Device Record Key | ab487915-0c42-4d8a-8f0b-e2ef3aa3902e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UniLite Universal Composite 4g B2 |
| Version Model Number | UL-B2 |
| Company DUNS | 532290720 |
| Company Name | D.S.I DENTAL SOLUTIONS LTD |
| 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 |