| Primary Device ID | 06932825300611 |
| NIH Device Record Key | 3de14502-519f-47cb-ada2-cb27de8557ed |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ethizo |
| Version Model Number | LS802-GP |
| Company DUNS | 679794078 |
| Company Name | Guangdong Transtek Medical Electronics 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| 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 | 06932825300611 [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 | 2022-10-28 |
| Device Publish Date | 2022-10-20 |
| 06932825304701 - ASTART | 2025-08-26 |
| 06932825304718 - ASTART | 2025-08-26 |
| 06932825304725 - ASTART | 2025-08-26 |
| 06932825304732 - ASTART | 2025-08-26 |
| 06932825304749 - ASTART | 2025-08-26 |
| 06932825303537 - CADENCE | 2025-07-29 |
| 06932825303155 - TeleRPM | 2025-07-23 |
| 06932825304565 - Brilliant Care | 2025-07-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ETHIZO 87597949 not registered Live/Pending |
DocToMe, Inc. 2017-09-06 |