| Primary Device ID | 00814913024677 |
| NIH Device Record Key | b2d60cbe-7e48-4167-9f45-409f4c7af2a6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET II Fixture SA Regular No-Mounted |
| Version Model Number | CET2R4511S |
| 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 | 00814913024677 [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 | 2017-11-17 |
| 00814913024776 | CET2R5015S |
| 00814913024769 | CET2R5013S |
| 00814913024752 | CET2R5011S |
| 00814913024745 | CET2R5010S |
| 00814913024738 | CET2R5008S |
| 00814913024721 | CET2R5007S |
| 00814913024714 | CET2R5006S |
| 00814913024691 | CET2R4515S |
| 00814913024684 | CET2R4513S |
| 00814913024677 | CET2R4511S |
| 00814913024660 | CET2R4510S |
| 00814913024653 | CET2R4508S |
| 00814913024646 | CET2R4507S |
| 00814913024639 | CET2R4018S |
| 00814913024622 | CET2R4015S |
| 00814913024615 | CET2R4013S |
| 00814913024608 | CET2R4011S |
| 00814913024592 | CET2R4010S |
| 00814913024585 | CET2R4008S |
| 00814913024578 | CET2R4007S |