| Primary Device ID | 19356870000038 |
| NIH Device Record Key | 1c40d584-82ee-433b-b967-0a02519c8c60 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CT:VQ |
| Version Model Number | 2.2.0 |
| Company DUNS | 747517097 |
| Company Name | 4DMEDICAL LIMITED |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| 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 |