| Primary Device ID | 14719846016504 |
| NIH Device Record Key | 981d5fd9-b43b-4cde-a5e8-b7021eca4b84 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Charder |
| Version Model Number | U310 |
| Company DUNS | 656102035 |
| Company Name | CHARDER ELECTRONIC CO., LTD. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04719846016507 [Primary] |
| GS1 | 14719846016504 [Package] Contains: 04719846016507 Package: CTN [4 Units] In Commercial Distribution |
| PUH | Analyzer, Body Composition, Exempt |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-08-20 |
| Device Publish Date | 2025-08-12 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CHARDER 77255412 3507248 Live/Registered |
Charder Electronic Co., Ltd. 2007-08-15 |
![]() CHARDER 77255368 3417917 Live/Registered |
Charder Electronic Co., Ltd. 2007-08-14 |
![]() CHARDER 76651560 not registered Dead/Abandoned |
CHARDER ELECTRONIC CO., LTD. 2005-12-07 |
![]() CHARDER 76651531 not registered Dead/Abandoned |
CHARDER ELECTRONIC CO., LTD. 2005-12-07 |