| Primary Device ID | 10810172700052 |
| NIH Device Record Key | 64e2b463-1e92-4958-a1e6-5aadf6da7805 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CASE-RDB-SpeedySwab Rapid COVID_19 + Flu A&B Antigen Self-Test 2 Tests/Box |
| Version Model Number | CASE-RDB-SpeedySwab Rapid COVID_19 + Flu A&B Antig |
| Company DUNS | 117617770 |
| Company Name | WatMIND USA |
| 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 | true |
| 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 | false |
| OTC Over-The-Counter | true |