| Primary Device ID | 00859882007634 |
| NIH Device Record Key | d74fe8c5-b3bf-4f9c-b291-56ecec5a7a6c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Procleix Zika Virus Assay |
| Version Model Number | 5K Kit Box 1 |
| Company DUNS | 056570085 |
| Company Name | GRIFOLS DIAGNOSTIC SOLUTIONS 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| 00859882007658 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |
| 00859882007641 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |
| 00859882007634 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |
| 00859882007504 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |
| 00859882007481 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |
| 00859882007474 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |
| 00859882007467 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |
| 00859882007450 | The Procleix Zika Virus Assay is a qualitative in vitro nucleic acid amplification test for the |