| Primary Device ID | 08800053045063 |
| NIH Device Record Key | de43063e-f551-43ad-af14-360c1573430e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LUVIS-C600 Series |
| Version Model Number | C600-E0S0A1 |
| Company DUNS | 694721181 |
| Company Name | DENTIS CO. ,LTD |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800053045063 [Primary] |
| EAZ | Light, Operating, Dental |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-31 |
| Device Publish Date | 2024-01-23 |
| 08800053053815 | AC 12-24 V, 50/60 Hz, 20-21 VA |
| 08800053053808 | AC 12-24 V, 50/60 Hz, 20-21 VA |
| 08800053053792 | AC 12-24 V, 50/60 Hz, 20-21 VA |
| 08800053053785 | AC 12-24 V, 50/60 Hz, 20-21 VA |
| 08800053045063 | AC 100-240 V, 50-60 Hz, 30-45 VA |
| 08800053045056 | AC 100-240 V, 50-60 Hz, 30-45 VA |
| 08800053045049 | AC 100-240 V, 50-60 Hz, 30-45 VA |
| 08800053045032 | AC 100-240 V, 50-60 Hz, 30-45 VA |