| Primary Device ID | 06953825905682 |
| NIH Device Record Key | a1575faf-dadf-407b-9806-df3bb1e496f4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PATIENT AID |
| Version Model Number | U80N |
| Company DUNS | 421294358 |
| Company Name | Shenzhen Urion 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 | 06953825905682 [Primary] |
| 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 | 2022-04-01 |
| Device Publish Date | 2022-03-24 |
| 16953825901070 - AlphaMed | 2025-09-08 |
| 16953825910041 - Alphamed | 2025-08-08 |
| 16953825909960 - N/A | 2025-07-10 |
| 16953825909953 - N/A | 2025-07-09 |
| 16953825909939 - Dr. Aid | 2025-07-07 |
| 16953825909892 - AlphaMed | 2025-06-30 |
| 16953825909878 - CuPiLO | 2025-06-23 |
| 16953825909885 - AlphaMed | 2025-06-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PATIENT AID 97026944 not registered Live/Pending |
PROFOUND HEALTH, LLC 2021-09-14 |
![]() PATIENT AID 87553616 5377296 Live/Registered |
Patient Aid 2017-08-03 |
![]() PATIENT AID 73274197 1194501 Dead/Cancelled |
Johnson & Johnson 1980-08-14 |