Primary Device ID | 16953825908789 |
NIH Device Record Key | 82eea7a7-21d8-4592-a93f-bb73df31b6f2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HEDIGON |
Version Model Number | U80AH |
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 | 06953825908782 [Primary] |
GS1 | 16953825908789 [Package] Contains: 06953825908782 Package: Carton [40 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 | 2024-10-14 |
Device Publish Date | 2024-10-06 |
16953825908772 - N/A | 2024-10-14 |
16953825908789 - HEDIGON | 2024-10-14 |
16953825908789 - HEDIGON | 2024-10-14 |
16953825908765 - ELERA | 2024-10-08 |
16953825908758 - Med One | 2024-09-30 |
16953825908734 - N/A | 2024-09-19 n/A |
16953825908659 - N/A | 2024-09-11 N/A |
16953825908697 - N/A | 2024-09-11 N/A |
16953825908666 - KARDIGI | 2024-09-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HEDIGON 90722313 not registered Live/Pending |
Guangzhou LiaoKang Medical Equipment Co.,Ltd. 2021-05-19 |