| Primary Device ID | 08800049429693 |
| NIH Device Record Key | d5253dd4-db3a-4c07-8b6a-6c209f4c91c6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UF(II) Implant System |
| Version Model Number | SSCA 75404H(II) |
| Catalog Number | SSCA 75404H(II) |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800049429693 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
[08800049429693]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-03-09 |
| Device Publish Date | 2022-03-01 |