| Primary Device ID | 08056771602723 |
| NIH Device Record Key | fb1adbe9-8c9a-4c90-8cc3-88ce29ed4910 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LIAISON Testosterone xt |
| Version Model Number | 318410 |
| Company DUNS | 033429783 |
| Company Name | Diasorin 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08056771602723 [Primary] |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-04-21 |
| Device Publish Date | 2021-04-13 |
| 08056771602945 - LIAISON QUANTIferon TB Gold Plus | 2023-09-18 USA manufactured kit |
| 08056771602952 - LIAISON Control QUANTIferon TB Gold Plus | 2023-09-18 USA manufactured control kit |
| 08056771600002 - LIAISON® Testosterone | 2023-05-03 |
| 08056771600019 - LIAISON® Testosterone Control Set | 2023-05-03 |
| 08056771602969 - LIAISON MeMed BV | 2022-08-18 The DiaSorin LIAISON MeMed BV is a semi-quantitative assay that uses chemiluminescent immunoassay (CLIA) technology to measure |
| 08056771602976 - LIAISON MeMed BV Control Set | 2022-08-18 The DiaSorin LIAISON MeMed BV Control Set is intended for use as assayed quality control samples to monitor the performance of t |
| 08056771602884 - LIAISON Q.S.E.T. Device Plus | 2022-08-17 Fecal extraction device |
| 08056771600590 - LIAISON Calprotectin | 2022-06-10 |