Primary Device ID | 16953825908840 |
NIH Device Record Key | d6fda360-c7ef-48c0-85c0-1a8d126a7c66 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AlphagoMed |
Version Model Number | U80EH |
Catalog Number | Yes |
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 | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06953825908843 [Primary] |
GS1 | 16953825908840 [Package] Contains: 06953825908843 Package: Carton [24 Units] 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 | 2024-11-01 |
Device Publish Date | 2024-10-24 |
06953825904593 | U81H |
06953825903435 | U80H |
06953825903169 | U60EH |
06953825903152 | U60CH |
06953825903145 | U80R |
06953825903138 | U80EH |
06953825904883 | U80E |
06953825909024 | U807 |
06953825903671 | U80K |
06953825903756 | U82H |
06953825903978 | U80U |
06953825904067 | U80RH |
06953825909055 | U81NH |
06953825909369 | U80M |
06953825907310 | U60BH |
06953825905323 | U80M |
06953825905859 | U80T |
16953825908840 | U80EH |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ALPHAGOMED 87374900 5363227 Live/Registered |
SHENZHENÂ URIONÂ TECHNOLOGYÂ CO.,LTD 2017-03-17 |