| Primary Device ID | 08800049453063 |
| NIH Device Record Key | c92c1539-c441-4f20-bcc9-4e18fc907d38 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UFIII Fixture |
| Version Model Number | UFIII 4013UV3 |
| Company DUNS | 631085206 |
| Company Name | DIO Corporation |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Lot Batch | true |
| Serial Number | true |
| 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 |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com | |
| Phone | 213-365-2875 |
| usahq@dioimplantusa.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800049453063 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-09-04 |
| Device Publish Date | 2023-08-25 |