| Primary Device ID | 16970784670700 |
| NIH Device Record Key | e964de86-fd4a-4787-ab3e-8ce3a669e9d4 |
| Commercial Distribution Discontinuation | 2020-12-20 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 01 |
| Company DUNS | 529870243 |
| Company Name | wenzhou dongfang medical instrument co.,ltd |
| 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 | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |