| Primary Device ID | 04719880531103 |
| NIH Device Record Key | ac7d2c95-a3b6-4b52-ac73-d55dc8184a6c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | QLoci |
| Version Model Number | md1000 Dx |
| Company DUNS | 658872364 |
| Company Name | LIFEOS GENOMICS CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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 | 04719880531103 [Primary] |
| NSU | Instrumentation For Clinical Multiplex Test Systems |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-05-08 |
| Device Publish Date | 2025-04-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() QLOCI 90027922 not registered Live/Pending |
LifeOS Genomics Corporation 2020-06-30 |