| Primary Device ID | 04719846007574 | 
| NIH Device Record Key | 7a0f2a98-4680-4480-a86c-7548257f57e8 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Charder | 
| Version Model Number | MS5900 | 
| 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 | true | 
| 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 | 04719846007574 [Primary] | 
| FRW | Scale, Patient | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2020-04-06 | 
| Device Publish Date | 2020-03-27 | 
| 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 |