| Primary Device ID | 00814913020327 |
| NIH Device Record Key | 8eb0740e-ce03-44eb-8f0b-9d4f043dee4a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET II Fixture SA Regular Pre-Mounted |
| Version Model Number | AET2R4011S |
| 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 | 00814913020327 [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 |
| 00814913020501 | AET2R5018S |
| 00814913020495 | AET2R5015S |
| 00814913020488 | AET2R5013S |
| 00814913020471 | AET2R5011S |
| 00814913020464 | AET2R5010S |
| 00814913020457 | AET2R5008S |
| 00814913020440 | AET2R5007S |
| 00814913020426 | AET2R4518S |
| 00814913020419 | AET2R4515S |
| 00814913020402 | AET2R4513S |
| 00814913020396 | AET2R4511S |
| 00814913020389 | AET2R4510S |
| 00814913020372 | AET2R4508S |
| 00814913020365 | AET2R4507S |
| 00814913020358 | AET2R4018S |
| 00814913020341 | AET2R4015S |
| 00814913020334 | AET2R4013S |
| 00814913020327 | AET2R4011S |
| 00814913020310 | AET2R4010S |
| 00814913020303 | AET2R4008S |
| 00814913020297 | AET2R4007S |