Primary Device ID | 04719846006935 |
NIH Device Record Key | 7597d401-7a10-4a02-9e07-96536405f12a |
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 | 04719846006935 [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 | 2020-03-09 |
Device Publish Date | 2020-03-01 |
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 |