| Primary Device ID | 06934440103066 |
| NIH Device Record Key | a88517ba-f1d6-4823-adc7-8e2c2d492db2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pulse Oximeter |
| Version Model Number | PO2 |
| Company DUNS | 421357243 |
| Company Name | Shenzhen Viatom Technology 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 |