Primary Device ID | 06953825910167 |
NIH Device Record Key | dbc7258f-d394-4285-b07f-07d17f9e094a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Holotis |
Version Model Number | U81E |
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 | 06953825910167 [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 | 2021-08-05 |
Device Publish Date | 2021-07-28 |
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 |
16953825909069 - N/A | 2024-12-10 |
16953825908994 - Aspire365 | 2024-12-06 |
16953825908970 - Alphamed | 2024-12-02 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HOLOTIS 90710551 not registered Live/Pending |
Dongguan Holotis Medical Co., Ltd. 2021-05-13 |