| Primary Device ID | 08806169098658 |
| NIH Device Record Key | 6df808c0-561a-41d8-acc8-279fda2212d9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DIOnavi-Denture |
| Version Model Number | 3DDEN-100 |
| Catalog Number | 3DDEN-100 |
| Company DUNS | 631085206 |
| Company Name | DIO Corporation |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08806169098658 [Primary] |
| EBI | Resin, Denture, Relining, Repairing, Rebasing |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2021-11-10 |
| Device Publish Date | 2020-11-05 |
| 08806169098672 | DIOnavi-Denture is a light-curable resin indicated for fabrication and repair of full and partia |
| 08806169098665 | DIOnavi-Denture is a light-curable resin indicated for fabrication and repair of full and partia |
| 08806169098658 | DIOnavi-Denture is a light-curable resin indicated for fabrication and repair of full and partia |