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 |
16953825908864 - Premier HEALTH SOLUTONS | 2024-11-04 |
16953825908871 - Mitdir | 2024-11-04 |
16953825908888 - Zybs Medical | 2024-11-04 |
16953825908840 - AlphagoMed | 2024-11-01 |
16953825908857 - Andesfit Health | 2024-11-01 |
16953825908833 - N/A | 2024-10-31 |
16953825908796 - urion | 2024-10-22 |
16953825908802 - urion | 2024-10-22 |
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 |