| Primary Device ID | 00810125991493 |
| NIH Device Record Key | 6a67cdc7-a055-4411-91b3-c30efce2445a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ET RIGID LAB ANALOG |
| Version Model Number | ETRLA471C |
| 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 | 00810125991493 [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 |
| 00810019240706 | ETRLA7005S |
| 00810019240690 | ETRLA6007S |
| 00810019240683 | ETRLA6005S |
| 00810019240676 | ETRLA6004S |
| 00810019240669 | ETRLA5007S |
| 00810019240652 | ETRLA5005S |
| 00810019240645 | ETRLA5004S |
| 00810019240638 | ETRLA4507 |
| 00810019240621 | ETRLA4505 |
| 00810019240614 | ETRLA4504 |
| 00810019240607 | ETRLA4007 |
| 00810019240591 | ETRLA4005 |
| 00810019240584 | ETRLA4004 |
| 00810125991561 | ETRLA760C |
| 00810125991554 | ETRLA670C |
| 00810125991547 | ETRLA660C |
| 00810125991530 | ETRLA640C |
| 00810125991516 | ETRLA560C |
| 00810125991509 | ETRLA540C |
| 00810125991493 | ETRLA471C |
| 00810125991486 | ETRLA461C |
| 00810125991479 | ETRLA441C |
| 00810125991462 | ETRLA470C |
| 00810125991455 | ETRLA460C |
| 00810125991448 | ETRLA440C |
| 00810125991523 | ETRLA570C |