| Primary Device ID | 06903053045216 |
| NIH Device Record Key | b370767d-f1fe-46a7-b50d-d7fdbbdb0034 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Resona A20 Pro Diagnostic Ultrasound System |
| Version Model Number | Resona A20 Pro |
| Company DUNS | 654671304 |
| Company Name | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| OTC Over-The-Counter | false |