| Primary Device ID | 00814913024882 |
| NIH Device Record Key | 780d5d96-4373-48b9-8fb8-253912d8ec01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET III SA Ultra-Wide Fixture No Mount |
| Version Model Number | CET3R6010S |
| Company DUNS | 796083090 |
| Company Name | HIOSSEN, INC. |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00814913024882 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-02-15 |
| 00814913024967 | CET3R7013S |
| 00814913024950 | CET3R7011S |
| 00814913024943 | CET3R7010S |
| 00814913024936 | CET3R7008S |
| 00814913024929 | CET3R7007S |
| 00814913024912 | CET3R7006S |
| 00814913024905 | AET3R6013S |
| 00814913024899 | CET3R6011S |
| 00814913024882 | CET3R6010S |
| 00814913024875 | CET3R6008S |
| 00814913024868 | CET3R6007S |
| 00814913024851 | CET3R6006S |
| 00810126045140 | CET3R7013S |
| 00810126045126 | CET3R7011S |
| 00810126045102 | CET3R7010S |
| 00810126045089 | CET3R7008S |
| 00810126045065 | CET3R7007S |
| 00810126045041 | CET3R7006S |
| 00810126045027 | CET3R6013S |
| 00810126045003 | CET3R6011S |
| 00810126044983 | CET3R6010S |
| 00810126044969 | CET3R6008S |
| 00810126044945 | CET3R6007S |
| 00810126044921 | CET3R6006S |