| Primary Device ID | 16974239700653 |
| NIH Device Record Key | d73f60e4-51ea-4e94-9ac6-1064bdb2a5b5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FOXXD |
| Version Model Number | ePA-13B4 |
| Company DUNS | 722481840 |
| Company Name | Guangzhou Daxin health 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06974239702872 [Primary] |
| GS1 | 16974239700653 [Package] Contains: 06974239702872 Package: [1 Units] Discontinued: 2024-08-01 Not in Commercial Distribution |
| GS1 | 26974239700650 [Package] Package: [10 Units] Discontinued: 2024-08-01 Not in Commercial Distribution |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-08-09 |
| Device Publish Date | 2024-08-01 |
| 16974239700653 | ePA-13B4 |
| 16974239700646 | TE-79 |
| 16974239700677 | EF-706B4 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FOXXD 88904369 not registered Live/Pending |
Foxx Development INC 2020-05-07 |
![]() FOXXD 88006121 5864015 Live/Registered |
Foxx Development Inc. 2018-06-19 |