| Primary Device ID | 06944904092980 |
| NIH Device Record Key | 9d250730-4e8d-4bf8-81d8-4fc6423c311d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | L12-4s Ultrasonic Probe Konica(FDA) |
| Version Model Number | 120-004755-00 |
| 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 | false |
| OTC Over-The-Counter | false |