| Primary Device ID | 16953825908857 |
| NIH Device Record Key | 1d4bc2f9-22a9-4143-91b6-5c99a00e40dd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Andesfit Health |
| Version Model Number | U80BH |
| 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 | 06953825908850 [Primary] |
| GS1 | 16953825908857 [Package] Contains: 06953825908850 Package: Carton [20 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 |
| 06953825903640 | U80L |
| 06953825905439 | U86E |
| 06953825905934 | U62I |
| 16953825906426 | UFR103 |
| 16953825908857 | U80BH |
| 16953825909076 | U60AH |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ANDESFIT HEALTH 90753515 not registered Live/Pending |
Andesfit System Limited 2021-06-03 |