| Primary Device ID | 18056771103401 |
| NIH Device Record Key | fcadcd63-1929-41a3-9a3e-2be2ecbf7180 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LIAISON XL MUREX HBeAg |
| Version Model Number | 318150 |
| Company DUNS | 630822989 |
| Company Name | DIASORIN SPA |
| 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 | 08056771103404 [Primary] |
| GS1 | 18056771103401 [Package] Contains: 08056771103404 Package: [10 Units] In Commercial Distribution |
| 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 |
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