| Primary Device ID | 00810125991189 |
| NIH Device Record Key | 3dfd18f9-dbb3-4b1b-9123-4c29dde938fa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET RIGID RETRACTION CAP |
| Version Model Number | ETRRC660C |
| 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 | false |
| 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 | 00810125991189 [Primary] |
| NDP | Accessories, Implant, Dental, Endosseous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-11 |
| Device Publish Date | 2024-07-03 |
| 00810019240348 | ETRRC760 |
| 00810019240331 | ETRRC670 |
| 00810019240324 | ETRRC660 |
| 00810019240317 | ETRRC640 |
| 00810019240300 | ETRRC570 |
| 00810019240294 | ETRRC560 |
| 00810019240287 | ETRRC540 |
| 00810019240270 | ETRRC471 |
| 00810019240263 | ETRRC461 |
| 00810019240256 | ETRRC441 |
| 00810019240249 | ETRRC470 |
| 00810019240232 | ETRRC460 |
| 00810019240225 | ETRRC440 |
| 00810125991097 | ETRRC460C |
| 00810125991080 | ETRRC440C |
| 00810125991202 | ETRRC760C |
| 00810125991196 | ETRRC670C |
| 00810125991189 | ETRRC660C |
| 00810125991172 | ETRRC640C |
| 00810125991165 | ETRRC570C |
| 00810125991158 | ETRRC560C |
| 00810125991141 | ETRRC540C |
| 00810125991134 | ETRRC471C |
| 00810125991127 | ETRRC461C |
| 00810125991110 | ETRRC441C |
| 00810125991103 | ETRRC470C |