| Primary Device ID | 06936415903862 |
| NIH Device Record Key | af104273-3e2c-4b35-9f42-320737e8b462 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 7L4A Ultrasonic Probe(V2.0/FDA) |
| Version Model Number | 120-007708-00 |
| 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 | true |
| OTC Over-The-Counter | false |