| Primary Device ID | 00814913020891 |
| NIH Device Record Key | 3a803a85-4614-4041-9703-2103bd044f5c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET III SA Ultra-Wide Fixture Pre-Mounted |
| Version Model Number | AET3R6013S |
| 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 | 00814913020891 [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 | 2015-09-01 |
| 00814913020952 | AET3R7013S |
| 00814913020945 | AET3R7011S |
| 00814913020938 | AET3R7010S |
| 00814913020921 | AET3R7008S |
| 00814913020914 | AET3R7007S |
| 00814913020907 | AET3R7006S |
| 00814913020891 | AET3R6013S |
| 00814913020884 | AET3R6011S |
| 00814913020877 | AET3R6010S |
| 00814913020860 | AET3R6008S |
| 00814913020853 | AET3R6007S |
| 00814913020846 | AET3R6006S |
| 00810126044204 | AET3R7013S |
| 00810126044181 | AET3R7011S |
| 00810126044167 | AET3R7010S |
| 00810126044143 | AET3R7008S |
| 00810126044129 | AET3R7007S |
| 00810126044105 | AET3R7006S |
| 00810126044082 | AET3R6013S |
| 00810126044068 | AET3R6011S |
| 00810126044044 | AET3R6010S |
| 00810126044020 | AET3R6008S |
| 00810126044006 | AET3R6007S |
| 00810126043986 | AET3R6006S |