| Primary Device ID | 00814913028927 |
| NIH Device Record Key | 66d52885-23ae-4442-aadc-722727317bfe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET IV Fixture SA Regular No Mount |
| Version Model Number | CET4R4508S |
| 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 | 00814913028927 [Primary] |
| DZE | Implant, Endosseous, Root-Form |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-07-18 |
| Device Publish Date | 2019-07-10 |
| 00814913029009 | CET4R5013S |
| 00814913028996 | CET4R5011S |
| 00814913028989 | CET4R5010S |
| 00814913028972 | CET4R5008S |
| 00814913028965 | CET4R5007S |
| 00814913028958 | CET4R4513S |
| 00814913028941 | CET4R4511S |
| 00814913028934 | CET4R4510S |
| 00814913028927 | CET4R4508S |
| 00814913028910 | CET4R4507S |
| 00814913028903 | CET4R4013S |
| 00814913028897 | CET4R4011S |
| 00814913028880 | CET4R4010S |
| 00814913028873 | CET4R4008S |
| 00814913028866 | CET4R4007S |