| Primary Device ID | 03661540600050 |
| NIH Device Record Key | 142c8f31-f97b-41f5-8a77-05211ec93d1a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Viva-E® |
| Version Model Number | 6002-380 |
| Company DUNS | 415733737 |
| Company Name | ELITechGroup B.V. |
| 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 | false |
| Lot Batch | false |
| 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 | 03661540600050 [Primary] |
| JJE | Analyzer, Chemistry (Photometric, Discrete), For Clinical Use |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-12-23 |
| Device Publish Date | 2016-11-21 |
| 03661540700064 - Excyte® | 2022-09-16 |
| 03661540700071 - Excyte® | 2022-09-16 |
| 03661540700118 - Excyte® | 2022-09-16 |
| 03661540700125 - Excyte® | 2022-09-16 |
| 03661540700446 - Excyte® | 2022-08-05 |
| 03661540700606 - Excyte® | 2021-12-28 |
| 03661540700613 - Excyte® | 2021-12-28 |
| 03661540700668 - Excyte® | 2021-12-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VIVA-E 76632811 3155685 Dead/Cancelled |
Dade Behring Inc. 2005-03-07 |