Primary Device ID | 16953825906884 |
NIH Device Record Key | 60c653d4-0824-49c3-a0e0-f58edb69e36c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Andesfit |
Version Model Number | U81E |
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 | 06953825906887 [Primary] |
GS1 | 16953825906884 [Package] Contains: 06953825906887 Package: Carton [30 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 | 2023-04-12 |
Device Publish Date | 2023-04-04 |
16953825909304 - carda health | 2025-01-20 |
16953825909281 - VtsniMed | 2025-01-14 |
16953825909243 - EVOLUTI | 2025-01-13 |
16953825909236 - COCACIS | 2025-01-09 |
16953825909168 - N/A | 2024-12-26 |
26953825909097 - santecare | 2024-12-25 |
16953825909076 - Andesfit Health | 2024-12-13 |
16953825909083 - Tovendor | 2024-12-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ANDESFIT 97820912 not registered Live/Pending |
Andesfit System Limited 2023-03-02 |
ANDESFIT 97820907 not registered Live/Pending |
Andesfit System Limited 2023-03-02 |