| Primary Device ID | 04952195344598 |
| NIH Device Record Key | 63bc0ba2-ad7c-47f8-9221-4c643541bd6d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Quolis 5000 Series Dental Unit |
| Version Model Number | AU-BDS5110 |
| Catalog Number | AU-BDS5110 |
| Company DUNS | 690540349 |
| Company Name | TAKARA-BELMONT CO., 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |