| Primary Device ID | B43071000030 |
| NIH Device Record Key | 677766a7-5b29-4550-bae7-03fa83ca9089 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GoCheck MultiScreener |
| Version Model Number | i15 Pro |
| Company DUNS | 035145840 |
| Company Name | Gobiquity, Inc. |
| 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 | false |
| 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 | true |
| OTC Over-The-Counter | false |