| Primary Device ID | 06946725526743 |
| NIH Device Record Key | fbd6dea0-0c33-4507-8aaf-80256e65c2f9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Blood pressure cuff |
| Version Model Number | A-XT-09 |
| Company DUNS | 529691989 |
| Company Name | APK Technology 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 | false |
| 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 | false |